Klein Test Bank Free Download 3rd Edition
Organic Chemistry 3rd Edition Klein Test Bank
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If you are looking for the full exam bank forKlein 3e or others, email us at [email protected] for more details. Cheers. Klein, Organic Chemistry 3e Chapter 5 one. What is the relationship between the following 2 compounds? A. constitutional isomers B. stereoisomers C. identical D. not isomers; unlike compounds entirely Respond: A Learning Objective: v.1 Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are practical to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Like shooting fish in a barrel two. What is the relationship between the following two compounds? A. ramble isomers B. stereoisomers C. identical D. non isomers; dissimilar compounds entirely Answer: C Learning Objective: 5.ane Compare ramble isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Like shooting fish in a barrel 3. What is the human relationship between the following two compounds? If yous are looking for the full test bank for Klein 3e or others, e-mail united states of america at [email protected] for more details. Cheers. A. constitutional isomers B. stereoisomers C. identical D. non isomers; different compounds entirely Answer: B Learning Objective: 5.1 Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are practical to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Piece of cake four. What is the relationship between the following two compounds? A. constitutional isomers B. stereoisomers C. identical D. not isomers; different compounds entirely Answer: B Learning Objective: 5.one Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Easy v. What is the relationship betwixt the post-obit two compounds? A. constitutional isomers B. stereoisomers C. identical If yous are looking for the full test bank for Klein 3e or others, electronic mail u.s.a. at [e-mail protected] for more details. Thanks. D. not isomers; different compounds entirely Respond: C Learning Objective: five.1 Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are practical to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Easy 6. What is the relationship between the following 2 compounds? A. constitutional isomers B. stereoisomers C. identical D. non isomers; different compounds entirely Answer: A Learning Objective: 5.1 Compare ramble isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Like shooting fish in a barrel 7. Is the post-obit alkene cis, trans, or neither? Reply: trans Learning Objective: 5.1 Compare constitutional isomers and stereoisomers, including an caption of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Like shooting fish in a barrel 8. Is the following alkene cis, trans, or neither? If you are looking for the full test bank for Klein 3e or others, email united states of america at [email protected] for more details. Thanks. Answer: neither Learning Objective: 5.one Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Easy 9. Is the post-obit alkene cis, trans, or neither? Answer: trans Learning Objective: 5.1 Compare ramble isomers and stereoisomers, including an caption of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Like shooting fish in a barrel ten. Is the following alkene cis, trans, or neither? Answer: cis Learning Objective: 5.i Compare ramble isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Easy 11. Is the following alkene cis, trans, or neither? If yous are looking for the full test bank for Klein 3e or others, email u.s.a. at [electronic mail protected] for more details. Thank you. Reply: neither Learning Objective: 5.1 Compare constitutional isomers and stereoisomers, including an caption of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Medium 12. Is the alkene on the left in the molecule below cis, trans, or neither? Respond: trans Learning Objective: v.1 Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Medium thirteen. Shown below is the structure of Crestor® (rosuvastatin), a medication used to reduce cholesterol. Is the highlighted alkene of rosuvastatin cis, trans, or neither? Reply: trans Learning Objective: v.1 Compare ramble isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Medium If you are looking for the full examination bank for Klein 3e or others, email us at [email protected] for more details. Cheers. xiv. Shown beneath is the structure of Singulair® (montelukast), a medication used to manage athsma. Is the alkene of montelukast cis, trans, or neither? Answer: trans Learning Objective: 5.1 Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Medium 15. Depict all the isomers with molecular formula C4H8. Answer: Learning Objective: 5.1 Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Hard xvi. Draw all the isomers with molecular formula C4H6. Answer: If y'all are looking for the full test banking concern for Klein 3e or others, email us at [e-mail protected] for more details. Cheers. Learning Objective: five.one Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Hard 17. Locate the chirality middle(s) in the following compound. Respond: Learning Objective: v.2 Describe the most common cause of chirality in a molecule, and depict a pair of enantiomers Difficulty: Medium eighteen. Shown below is the construction of the drug nicotine. Locate the chirality middle(due south) in the following compound. Reply: If y'all are looking for the full test banking company for Klein 3e or others, email united states of america at [email protected] for more details. Thanks. Learning Objective: 5.ii Describe the nigh common cause of chirality in a molecule, and draw a pair of enantiomers Difficulty: Easy 19. Locate the chirality middle(s) in the post-obit compound. Reply: Learning Objective: 5.2 Describe the most common cause of chirality in a molecule, and depict a pair of enantiomers Difficulty: Easy twenty. Locate the chirality middle(s) in the following chemical compound. Answer: If you are looking for the total test bank for Klein 3e or others, email us at [email protected] for more details. Thanks. Learning Objective: 5.2 Describe the almost mutual crusade of chirality in a molecule, and draw a pair of enantiomers Difficulty: Like shooting fish in a barrel 21. Locate the chirality center(due south) in the following compound. Answer: Learning Objective: 5.2 Describe the most common cause of chirality in a molecule, and draw a pair of enantiomers Difficulty: Easy 22. Place the relationship between the post-obit ii structures. A. enantiomers B. identical C. neither If y'all are looking for the total test bank for Klein 3e or others, e-mail united states of america at [email protected] for more details. Thanks. Reply: B Learning Objective: 5.2 Depict the most common cause of chirality in a molecule, and draw a pair of enantiomers Difficulty: Easy 23. Place the relationship between the following 2 structures. A. enantiomers B. identical C. neither Answer: A Learning Objective: 5.ii Draw the most common crusade of chirality in a molecule, and draw a pair of enantiomers Difficulty: Easy 24. Place the human relationship betwixt the following ii structures. A. enantiomers B. identical C. neither Answer: B Learning Objective: 5.2 Describe the most common cause of chirality in a molecule, and draw a pair of enantiomers Difficulty: Easy 25. Place the relationship betwixt the following two structures. If y'all are looking for the full test banking company for Klein 3e or others, email u.s.a. at [email protected] for more details. Thanks. A. enantiomers B. identical C. neither Respond: A Learning Objective: 5.2 Describe the almost mutual crusade of chirality in a molecule, and draw a pair of enantiomers Difficulty: Like shooting fish in a barrel 26. Identify the relationship betwixt the following two structures. A. enantiomers B. identical C. neither Answer: B Learning Objective: 5.2 Depict the nearly mutual crusade of chirality in a molecule, and describe a pair of enantiomers Difficulty: Medium 27. Describe the enantiomer of the following compound. Answer: If you lot are looking for the full test bank for Klein 3e or others, email us at [e-mail protected] for more details. Thank you. Learning Objective: v.ii Draw the most mutual cause of chirality in a molecule, and draw a pair of enantiomers Difficulty: Medium 28. Draw the enantiomer of the post-obit compound. Answer: Learning Objective: 5.ii Describe the most common cause of chirality in a molecule, and depict a pair of enantiomers Difficulty: Medium 29. Draw the enantiomer of the following chemical compound. Answer: If you are looking for the total test banking company for Klein 3e or others, email us at [email protected] for more details. Thanks. Learning Objective: 5.2 Draw the near mutual cause of chirality in a molecule, and describe a pair of enantiomers Difficulty: Medium thirty. Draw the enantiomer of the following compound. Answer: Learning Objective: v.2 Describe the most common cause of chirality in a molecule, and draw a pair of enantiomers Difficulty: Medium 31. Draw the enantiomer of the following chemical compound. Reply: If you are looking for the full exam bank for Klein 3e or others, electronic mail united states of america at [e-mail protected] for more than details. Cheers. Learning Objective: 5.ii Describe the nearly common cause of chirality in a molecule, and draw a pair of enantiomers Difficulty: Medium 32. Assign the absolute configuration of the chirality center as R or S. Answer: S Learning Objective: five.3 Depict how the configuration of a chirality centre is assigned using the Cahn-Ingold-Prelog arrangement Difficulty: Easy 33. Assign the absolute configuration of the chirality center as R or S. Answer: S Learning Objective: 5.3 Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog organisation Difficulty: Piece of cake 34. Assign the absolute configuration of the chirality center as R or S. If you are looking for the full test bank for Klein 3e or others, electronic mail u.s.a. at [email protected] for more details. Thanks. Reply: R Learning Objective: 5.iii Draw how the configuration of a chirality heart is assigned using the Cahn-Ingold-Prelog system Difficulty: Piece of cake 35. Assign the accented configuration of the chirality center as R or S. Answer: Due south Learning Objective: v.3 Describe how the configuration of a chirality eye is assigned using the Cahn-Ingold-Prelog system Difficulty: Easy 36. Assign the accented configuration of the chirality center as R or S. Reply: R Learning Objective: v.three Draw how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog organization Difficulty: Like shooting fish in a barrel 37. Assign the accented configuration of the chirality center as R or S. If you lot are looking for the full examination bank for Klein 3e or others, electronic mail us at [e-mail protected] for more details. Thanks. Respond: R Learning Objective: five.iii Draw how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Piece of cake 38. Drawn beneath is the construction of Crestor® (rosuvastatin), a medication used to reduce cholesterol. Assign the accented configurations of the 2 chirality centers as R or S. Answer: Left (allylic) alcohol is S; right alcohol is R Learning Objective: v.3 Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 39. Fatigued below is the structure of Singulair® (montelukast), a medication used to manage athsma. Assign the accented configuration of the chirality middle as R or Southward. Answer: R Learning Objective: five.three Describe how the configuration of a chirality centre is assigned using the Cahn-Ingold-Prelog arrangement Difficulty: Medium If y'all are looking for the full test depository financial institution for Klein 3e or others, email u.s. at [email protected] for more details. Thanks. 40. Drawn below is the structure of Plavix® (clopidogrel), a medication used to manage claret clots. Assign the absolute configuration of the chirality center as R or S. Answer: Due south Learning Objective: five.3 Draw how the configuration of a chirality eye is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 41. Drawn below is the construction of Cymbalta® (duloxetine), a medication used to manage depression. Assign the accented configuration of the chirality center every bit R or S. Respond: S Learning Objective: 5.iii Describe how the configuration of a chirality centre is assigned using the Cahn-Ingold-Prelog arrangement Difficulty: Medium 42. Provide an IUPAC name of the post-obit compound. Answer: (Southward)-iv-methyl-2-pentanol If yous are looking for the full test bank for Klein 3e or others, email us at [email protected] for more than details. Thanks. Learning Objective: v.iii Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 43. Provide an IUPAC proper name of the following compound. Reply: (S)-3-octanol Learning Objective: v.3 Describe how the configuration of a chirality heart is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 44. Which of the following is the right structure for the compound (R)-2-pentanol? A. I B. 2 C. III D. 4 Reply: C Learning Objective: 5.3 Draw how the configuration of a chirality heart is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 45. Which of the following is the right construction for the compound (South)-3- methylheptane. If yous are looking for the full test bank for Klein 3e or others, email u.s.a. at [email protected] for more details. Thanks. A. I B. Ii C. III D. 4 Answer: B Learning Objective: five.3 Depict how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 46. Draw the structure of the compound (Southward)-iii-methylheptane. Answer: Learning Objective: five.3 Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 47. Draw the structure of the compound (R)-4-ethyloctane. Answer: Learning Objective: 5.3 Draw how the configuration of a chirality eye is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium If y'all are looking for the total exam bank for Klein 3e or others, email united states of america at [e-mail protected] for more than details. Thanks. 48. Which of the following is the correct IUPAC proper name of the following structure? A. (S)-3-ethyl-ii-methylhexane B. (R)-3-ethyl-2-methylhexane C. (S)-iii-ethyl-2-methylpentane D. (R)-iii-ethyl-2-methylpentane Answer: B Learning Objective: 5.three Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Medium 49. Which of the following is the correct IUPAC name of the post-obit structure? A. (South)-2-ethylhexane B. (Southward)-iii-methylheptane C. (R)-2-ethylhexane D. (R)-3-methylheptane Reply: D Learning Objective: 5.3 Describe how the configuration of a chirality centre is assigned using the Cahn-Ingold-Prelog organisation Difficulty: Medium 50. Redraw the structure below equally a wedge-dash construction and label any/all stereocenters with their absolute configuration. Reply: If you are looking for the full test bank for Klein 3e or others, electronic mail us at [electronic mail protected] for more than details. Thank you. Learning Objective: five.iii Describe how the configuration of a chirality middle is assigned using the Cahn-Ingold-Prelog system Difficulty: Hard 51. Redraw the construction below equally a wedge-nuance construction and label all stereocenters with their absolute configuration. Answer: Learning Objective: v.iii Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Hard 52. Identify the human relationship betwixt these two structures. If yous are looking for the full test bank for Klein 3e or others, electronic mail united states of america at [email protected] for more than details. Thanks. A. diastereomers B. enantiomers C. the same compound D. different compounds Reply: A Learning Objective: 5.3 Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Hard 53. Rank the following from highest to lowest priority according to the Cahn-Ingold- Prelog system. I. -F 2. -H Three. -OH Four. -SH Answer: IV > I > Iii > Ii Learning Objective: five.three Describe how the configuration of a chirality eye is assigned using the Cahn-Ingold-Prelog system Difficulty: Easy 54. Rank the following from highest to lowest priority according to the Cahn-Ingold- Prelog organization. I. -CH3 Two. -CN Three. -CH2OH IV. -Br Answer: IV > Three > 2 > I Learning Objective: 5.iii Draw how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Easy 55. Rank the following from highest to lowest priority co-ordinate to the Cahn-Ingold- Prelog organisation. I. -CH2CH3 II. -CHCH2 III. -CCH IV. -CH3 Respond: Iii > II > I > IV Learning Objective: v.3 Describe how the configuration of a chirality center is assigned using the Cahn-Ingold-Prelog system Difficulty: Like shooting fish in a barrel If you are looking for the full test bank for Klein 3e or others, electronic mail usa at [email protected] for more than details. Thanks. 56. What is the % ee of a sample of carvone that exhibits a specific rotation of −20, given that the specific rotation of (R)-carvone is −61? Reply: 33% Learning Objective: v.4 Compare the effects of a pair of enantiomers on aeroplane- polarized light, discussing how the relative amounts of the two enantiomers affect the observed rotation of plane-polarized light Difficulty: Medium 57. What is the % ee of a sample of carvone that exhibits a specific rotation of −40, given that the specific rotation of (R)-carvone is −61? Answer: 66% Learning Objective: five.4 Compare the effects of a pair of enantiomers on plane- polarized light, discussing how the relative amounts of the 2 enantiomers touch on the observed rotation of plane-polarized calorie-free Difficulty: Medium 58. If a sample of carvone gives a specific rotation of −60 and the specific rotation of (R)-carvone is −61, does the unknown sample primarily have the R or South absolute configuration? Reply: R Learning Objective: 5.4 Compare the effects of a pair of enantiomers on plane- polarized light, discussing how the relative amounts of the two enantiomers touch the observed rotation of plane-polarized light Difficulty: Medium 59. If a sample of carvone gives a specific rotation of 0 and the specific rotation of pure (R)-carvone is −61, what is the configuration of the unknown sample? Answer: neither, it is a racemic mixture Learning Objective: 5.four Compare the furnishings of a pair of enantiomers on airplane- polarized light, discussing how the relative amounts of the ii enantiomers impact the observed rotation of plane-polarized light Difficulty: Medium If you are looking for the full test depository financial institution for Klein 3e or others, email united states of america at [email protected] for more details. Thanks. 60. What is the specific rotation of pure (S)-carvone if a sample of (R)-carvone of 85% ee has a specific rotation of −52? A. −61 B. 64 C. 0 D. 61 Answer: D Learning Objective: 5.4 Compare the effects of a pair of enantiomers on plane- polarized lite, discussing how the relative amounts of the two enantiomers affect the observed rotation of plane-polarized lite Difficulty: Medium 61. What is the specific rotation of a sample of carvone that is an equal mixture of the R and S enantiomers? (R)- carvone has a specific rotation of −61. A. −61 B. 64 C. 0 D. 61 Answer: C Learning Objective: 5.four Compare the effects of a pair of enantiomers on plane- polarized light, discussing how the relative amounts of the two enantiomers affect the observed rotation of plane-polarized low-cal Difficulty: Medium 62. What is the per centum of the R enantiomer in a sample of carvone that has a specific rotation of 10, given that the specific rotation of (R)-carvone is −61? A. 42 B. 84 C. 16 D. 58 Answer: D If yous are looking for the total test bank for Klein 3e or others, electronic mail us at [email protected] for more details. Thanks. Learning Objective: 5.4 Compare the effects of a pair of enantiomers on airplane- polarized light, discussing how the relative amounts of the two enantiomers impact the observed rotation of plane-polarized lite Difficulty: Hard 63. What is the percentage of the R enantiomer in a sample of carvone that has a specific rotation of 30, given that the specific rotation of (R)-carvone is −61? A. 26% B. 51% C. 49% D. 75% Reply: A Learning Objective: v.4 Compare the effects of a pair of enantiomers on aeroplane- polarized light, discussing how the relative amounts of the ii enantiomers bear upon the observed rotation of aeroplane-polarized light Difficulty: Medium 64. What is the percentage of the Southward enantiomer in a sample of carvone that has a specific rotation of 10, given that the specific rotation of (R)-carvone is −61? A. 42 B. 84 C. 16 D. 58 Reply: A Learning Objective: 5.four Compare the effects of a pair of enantiomers on plane- polarized light, discussing how the relative amounts of the 2 enantiomers affect the observed rotation of plane-polarized light Difficulty: Hard 65. What is the per centum of the Southward enantiomer in a sample of carvone that has a specific rotation of thirty, given that the specific rotation of (R)-carvone is −61? A. 25.five% B. 51% If you lot are looking for the full examination bank for Klein 3e or others, email us at [e-mail protected] for more details. Thanks. C. 49% D. 74.5% Reply: D Learning Objective: 5.iv Compare the effects of a pair of enantiomers on airplane- polarized lite, discussing how the relative amounts of the two enantiomers affect the observed rotation of plane-polarized light Difficulty: Medium 66. What is the per centum of the R enantiomer in a sample of carvone that has a specific rotation of −20, given that the specific rotation of (R)-carvone is −61? A. 20% B. 66.5% C. 33.five% D. 61% Answer: B Learning Objective: 5.4 Compare the effects of a pair of enantiomers on plane- polarized lite, discussing how the relative amounts of the 2 enantiomers affect the observed rotation of plane-polarized light Difficulty: Medium 67. What is the pct of the R enantiomer in a sample of limonene that has a specific rotation of −38, given that the specific rotation of (S)-limonene is −116? Reply: 66% Learning Objective: 5.4 Compare the effects of a pair of enantiomers on plane- polarized lite, discussing how the relative amounts of the ii enantiomers bear upon the observed rotation of aeroplane-polarized light Difficulty: Medium 68. The structure of Crestor (rosuvastatin), a medication used to reduce cholesterol, is shown beneath. If the specific rotation for this compound is known to be +100, what would be the specific rotation for the stereoisomer shown at the right? If you lot are looking for the full test bank for Klein 3e or others, email usa at [e-mail protected] for more details. Thanks. A. +100 B. -100 C. 0 D. Impossible to predict Answer: D Learning Objective: 5.4 Compare the effects of a pair of enantiomers on aeroplane- polarized light, discussing how the relative amounts of the two enantiomers bear upon the observed rotation of plane-polarized lite Difficulty: Medium 69. What is the human relationship of the following two structures? A. enantiomers B. diastereomers C. constitutional isomers D. identical Answer: B Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a compound tin have Difficulty: Medium If yous are looking for the total exam bank for Klein 3e or others, email u.s. at [email protected] for more than details. Thanks. 70. What is the relationship of the following ii structures? A. enantiomers B. diastereomers C. constitutional isomers D. identical Respond: A Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a compound tin have Difficulty: Medium 71. What is the relationship of the following two structures? A. enantiomers B. diastereomers C. constitutional isomers D. identical Reply: A Learning Objective: 5.v Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound tin can have Difficulty: Medium 72. What is the relationship of the following two structures? If you are looking for the full test depository financial institution for Klein 3e or others, email us at [email protected] for more details. Thanks. A. enantiomers B. diastereomers C. ramble isomers D. identical Answer: D Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a compound tin take Difficulty: Medium 73. What is the relationship of the following 2 structures? A. enantiomers B. diastereomers C. constitutional isomers D. identical Answer: B Learning Objective: five.v Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can have Difficulty: Medium 74. Draw the enantiomer of the following compound. If yous are looking for the full test bank for Klein 3e or others, electronic mail us at [email protected] for more details. Thanks. Respond: Learning Objective: 5.five Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can have Difficulty: Medium 75. Draw the enantiomer of the following compound. Answer: none. There is no stereocenter, so the chemical compound is not chiral and thus does not have an enantiomer. Learning Objective: five.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a compound can accept Difficulty: Medium 76. Describe the enantiomer of the following chemical compound. Answer: Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can have If you are looking for the full test bank for Klein 3e or others, electronic mail u.s.a. at [email protected] for more details. Thanks. Difficulty: Medium 77. Depict a diastereomer of the following compound. Reply: Learning Objective: v.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can take Difficulty: Difficult 78. Draw a diastereomer of the post-obit chemical compound. Answer: None. There is only i stereocenter, so the compound does not have a diastereomer. Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can have Difficulty: Hard 79. Describe a diastereomer of the following compound. If you are looking for the full test bank for Klein 3e or others, email us at [email protected] for more details. Thanks. Reply: Learning Objective: five.v Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can have Difficulty: Difficult 80. Draw all the stereoisomers of the post-obit compound. Reply: Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can have Difficulty: Difficult 81. Draw all the stereoisomers of the following compound. Answer: If you are looking for the full test bank for Klein 3e or others, email us at [electronic mail protected] for more than details. Cheers. Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a chemical compound can have Difficulty: Hard 82. Which of the post-obit choices is a diastereomer of the first construction shown? A. I B. 2 C. 3 D. IV Answer: C Learning Objective: v.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a compound tin can accept Difficulty: Medium 83. Which of the following choices is a diastereomer of the beginning structure shown. If yous are looking for the full test bank for Klein 3e or others, email united states at [email protected] for more than details. Thanks. A. I B. 2 C. III D. Iv Reply: D Learning Objective: 5.5 Compare stereoisomers with diastereomers, explaining how many stereoisomers a compound tin can have Difficulty: Medium 84. Which of the post-obit choices is a diastereomer of the beginning structure shown? A. I B. Two If yous are looking for the full test bank for Klein 3e or others, electronic mail u.s.a. at [email protected] for more than details. Thanks. C. Three D. IV Answer: B Learning Objective: 5.v Compare stereoisomers with diastereomers, explaining how many stereoisomers a compound can have Difficulty: Medium 85. Is the following a meso chemical compound? Answer: No Learning Objective: v.6 Compare rotational and reflectional symmetry, discussing if and how an centrality of symmetry and plane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Medium 86. Which of the following can be as a meso isomer? A. I B. II C. Three D. Four Answer: A Learning Objective: 5.6 Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and plane of symmetry affects chirality and whether a meso compound is chiral or achiral If you are looking for the full examination bank for Klein 3e or others, electronic mail u.s.a. at [email protected] for more details. Cheers. Difficulty: Medium 87. Does the post-obit comprise a plane of symmetry? Answer: yes Learning Objective: v.half dozen Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and plane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Piece of cake 88. Draw in the airplane of symmetry in the post-obit chemical compound. Answer: Learning Objective: 5.6 Compare rotational and reflectional symmetry, discussing if and how an centrality of symmetry and plane of symmetry affects chirality and whether a meso chemical compound is chiral or achiral Difficulty: Easy 89. Draw in the plane of symmetry in the post-obit compound. If you are looking for the total exam bank for Klein 3e or others, email us at [email protected] for more details. Cheers. Reply: none Learning Objective: five.vi Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and plane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Hard 90. Draw all of the possible stereoisomers of the following compound. Answer: 7 Learning Objective: 5.6 Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and airplane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Hard 91. How many stereoisomers are possible for ii,three-dimethylbutane? Answer: None. It has no stereocenters. Learning Objective: 5.vi Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and plane of symmetry affects chirality and whether a meso chemical compound is chiral or achiral Difficulty: Hard 92. Draw all possible stereoisomers of 1,3,v-trimethylcyclohexane. If you are looking for the full test bank for Klein 3e or others, email us at [electronic mail protected] for more details. Thanks. Respond: Learning Objective: 5.6 Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and airplane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Medium 93. Depict the meso isomer of the post-obit compound. Answer: Learning Objective: five.6 Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and aeroplane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Hard 94. Draw the meso isomer of the post-obit chemical compound. If you are looking for the full test depository financial institution for Klein 3e or others, email us at [email protected] for more details. Thanks. Respond: Learning Objective: 5.6 Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and plane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Hard 95. Draw the meso isomer of the following compound. Answer: Learning Objective: five.half-dozen Compare rotational and reflectional symmetry, discussing if and how an centrality of symmetry and plane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Medium 96. How many possible stereoisomers are there for Crestor ® (rosuvastatin), a medication used to reduce cholesterol? If you are looking for the full test bank for Klein 3e or others, electronic mail usa at [email protected] for more details. Thank you. A. two B. 4 C. 6 D. 8 Respond: D Learning Objective: 5.6 Compare rotational and reflectional symmetry, discussing if and how an axis of symmetry and aeroplane of symmetry affects chirality and whether a meso compound is chiral or achiral Difficulty: Hard 97. Depict the Fischer projection of the post-obit compound. Respond: Learning Objective: 5.vii Draw a Fischer projection of glucose or some other sugar Difficulty: Difficult 98. Depict the Fischer projection of the post-obit compound. If yous are looking for the full test depository financial institution for Klein 3e or others, email usa at [e-mail protected] for more than details. Thanks. Answer: Learning Objective: 5.7 Describe a Fischer project of glucose or some other sugar Difficulty: Hard 99. Describe the Fischer projection of the following compound. Answer: Learning Objective: 5.vii Depict a Fischer projection of glucose or another sugar Difficulty: Hard 100. Draw the Fischer projection of the following chemical compound. If yous are looking for the full exam depository financial institution for Klein 3e or others, email usa at [e-mail protected] for more details. Thanks. Respond: Learning Objective: five.7 Draw a Fischer projection of glucose or another sugar Difficulty: Difficult 101. Convert the following Fischer projection into a wedge/dash cartoon. Respond: Learning Objective: 5.7 Draw a Fischer projection of glucose or another sugar Difficulty: Hard 102. Catechumen the following Fischer projection into a wedge/dash cartoon. If you lot are looking for the full test banking concern for Klein 3e or others, email us at [e-mail protected] for more details. Thanks. Answer: Learning Objective: 5.7 Depict a Fischer projection of glucose or another sugar Difficulty: Hard 103. Catechumen the post-obit Fischer projection into a wedge/dash drawing. Answer: Learning Objective: 5.7 Draw a Fischer projection of glucose or some other sugar Difficulty: Hard 104. Convert the following Fischer projection into a wedge/nuance drawing. If you are looking for the full test banking company for Klein 3e or others, email us at [email protected] for more details. Thanks. Answer: Learning Objective: v.seven Draw a Fischer projection of glucose or another sugar Difficulty: Difficult 105. Which of the following is a correct Fischer projection of the following compound? A. I B. II C. III D. Four Answer: A Learning Objective: 5.vii Draw a Fischer projection of glucose or another sugar Difficulty: Hard If you are looking for the full examination banking concern for Klein 3e or others, electronic mail us at [email protected] for more details. Cheers. 106. Which of the post-obit is a correct Fischer projection of the following compound? A. I B. II C. 3 D. IV Answer: C Learning Objective: 5.7 Draw a Fischer projection of glucose or some other sugar Difficulty: Hard 107. Which of the following is a correct Fischer projection of the following compound? If you are looking for the total test bank for Klein 3e or others, email us at [email protected] for more than details. Thanks. A. I B. II C. 3 D. IV Answer: A Learning Objective: five.7 Draw a Fischer project of glucose or another carbohydrate Difficulty: Hard 108. Which of the following structures is the correct wedge/nuance drawing of the following Fischer projection? A. I B. Ii C. 3 D. Four If you are looking for the full test bank for Klein 3e or others, e-mail united states of america at [e-mail protected] for more details. Thanks. Reply: B Learning Objective: 5.7 Depict a Fischer projection of glucose or another sugar Difficulty: Hard 109. Which of the following structures is a correct wedge/dash drawing of the following Fischer projection? A. I B. 2 C. 3 D. IV Answer: B Learning Objective: 5.vii Draw a Fischer projection of glucose or another sugar Difficulty: Difficult 110. What is the relationship between the following two molecules? If yous are looking for the full examination depository financial institution for Klein 3e or others, email us at [email protected] for more details. Thanks. A. enantiomers B. diastereomers C. identical D. ramble Isomers Answer: A Learning Objective: 5.vii Draw a Fischer projection of glucose or another sugar Difficulty: Like shooting fish in a barrel 111. What is the relationship between the post-obit two molecules? A. enantiomers B. diastereomers C. identical D. constitutional Isomers Reply: B Learning Objective: five.7 Draw a Fischer projection of glucose or another sugar Difficulty: Easy 112. What is the human relationship between the following 2 molecules? A. enantiomers If you lot are looking for the full test depository financial institution for Klein 3e or others, email u.s.a. at [e-mail protected] for more than details. Thanks. B. diastereomers C. identical D. constitutional Isomers Answer: C Learning Objective: 5.7 Depict a Fischer projection of glucose or another carbohydrate Difficulty: Medium 113. Assign the post-obit stereocenter as having the R or S absolute configuration. Reply: S Learning Objective: five.seven Draw a Fischer project of glucose or another carbohydrate Difficulty: Medium 114. Assign the following stereocenter as having the R or S absolute configuration. Answer: South Learning Objective: 5.7 Draw a Fischer projection of glucose or another saccharide Difficulty: Hard 115. Assign the following stereocenter as having the R or S absolute configuration. Answer: Neither – no stereocenter Learning Objective: 5.7 Draw a Fischer projection of glucose or another sugar Difficulty: Medium If yous are looking for the total test bank for Klein 3e or others, electronic mail usa at [electronic mail protected] for more details. Thank you. 116. Provide an IUPAC name for the following compound. Reply: (R)-two-butanol Learning Objective: v.7 Draw a Fischer projection of glucose or another sugar Difficulty: Medium 117. Which of the following is the IUPAC name for the post-obit compound? A. (South)-two-pentanol B. (S)-2-butanol C. (R)-2-pentanol D. (R)-2-butanol Answer: A Learning Objective: v.7 Draw a Fischer projection of glucose or another sugar Difficulty: Difficult 118. Identify the relationship between these two structures. A. diastereomers If you are looking for the full examination bank for Klein 3e or others, electronic mail us at [electronic mail protected] for more than details. Cheers. B. enantiomers C. identical D. unrelated compounds Respond: C. Learning Objective: 5.vii Draw a Fischer project of glucose or another sugar Difficulty: Hard 119. What is the relationship between the ii structures shown? A. identical B. enantiomers C. diastereomers D. none of these Answer: A Learning Objective: 5.eight Describe conformationally mobile systems Difficulty: Difficult 120. What is the relationship between the two structures shown? A. same compound B. enantiomers C. diastereomers D. none of these Answer: B Learning Objective: 5.eight Describe conformationally mobile systems Difficulty: Hard If you are looking for the full exam bank for Klein 3e or others, electronic mail u.s. at [email protected] for more details. Thanks. 121. What is the human relationship between the two structures shown? A. same compound B. enantiomers C. diastereomers D. none of these Reply: C Learning Objective: 5.8 Describe conformationally mobile systems Difficulty: Hard 122. What is the relationship betwixt the two structures shown? A. same chemical compound B. enantiomers C. diastereomers D. none of these Respond: D Learning Objective: 5.viii Describe conformationally mobile systems Difficulty: Hard 123. What is the relationship between the 2 structures shown? If yous are looking for the full test banking concern for Klein 3e or others, email united states at [email protected] for more than details. Thanks. A. same compound B. enantiomers C. diastereomers D. none of these Respond: C Learning Objective: 5.8 Draw conformationally mobile systems Difficulty: Difficult 124. Stereoisomers that result from the hindered rotation of a single bond are called ___________. Answer: atropisomers Learning Objective: v.ix Discuss ways in which a compound tin be chiral without containing a chiral centre Difficulty: Medium 125. What is the relationship betwixt the two structures shown? A. same compound B. enantiomers C. diastereomers D. none of these Answer: B Learning Objective: 5.9 Discuss ways in which a chemical compound can be chiral without containing a chiral center Difficulty: Medium If you are looking for the total test bank for Klein 3e or others, email us at [electronic mail protected] for more details. Thanks. 126. Identify the hybridization of the centre carbon of an allene. A. sp B. sp2 C. sp3 D. sp4 Answer: A Learning Objective: v.9 Discuss ways in which a compound can be chiral without containing a chiral center Difficulty: Medium 127. Which of the post-obit strategies will NOT be an constructive way to separate enantiomers? A. chiral chromatography B. distillation C. crystallization D. chiral resolving agents Answer: B Learning Objective: 5.10 Describe resolution and methods to separate enantiomers Difficulty: Medium 128. When a racemic mixture is reacted with a unmarried enantiomer of another chemical compound, so a pair of _________ is formed. A. identical compounds B. enantiomers C. diastereomers D. none of the higher up Answer: B Learning Objective: 5.10 Draw resolution and methods to separate enantiomers Difficulty: Medium 129. In chiral column chromatography, __________ adsorbent is used to separate a pair of enantiomers. If you are looking for the full test bank for Klein 3e or others, e-mail us at [electronic mail protected] for more details. Thank you. A. an achiral B. a polar C. a nonpolar D. a chiral Reply: D Learning Objective: v.10 Describe resolution and methods to dissever enantiomers Difficulty: Medium 130. Is the post-obit alkene E, Z, or neither? Reply: E Learning Objective: five.11 Describe how stereodiscriptors are assigned for certain trisubstituted and tetrasubstituted alkenes Difficulty: Medium 131. Is the following alkene E, Z, or neither? Respond: neither Learning Objective: 5.11 Draw how stereodiscriptors are assigned for certain trisubstituted and tetrasubstituted alkenes Difficulty: Medium 132. Is the following alkene E, Z, or neither? Reply: E If you are looking for the full test banking concern for Klein 3e or others, email us at [electronic mail protected] for more details. Thanks. Learning Objective: 5.11 Draw how stereodiscriptors are assigned for certain trisubstituted and tetrasubstituted alkenes Difficulty: Medium 133. Is the following alkene Eastward, Z, or neither? Answer: Z Learning Objective: v.xi Draw how stereodiscriptors are assigned for certain trisubstituted and tetrasubstituted alkenes Difficulty: Medium 134. Is the following alkene Due east, Z, or neither? Answer: neither Learning Objective: 5.eleven Describe how stereodiscriptors are assigned for sure trisubstituted and tetrasubstituted alkenes Difficulty: Medium 135. Is the alkene on the left in the molecule below E, Z, or neither? Reply: E Learning Objective: five.eleven Depict how stereodiscriptors are assigned for certain trisubstituted and tetrasubstituted alkenes Difficulty: Medium If you are looking for the full test depository financial institution for Klein 3e or others, email us at [email protected] for more details. Thanks. 136. Is the post-obit alkene E, Z, or neither? Answer: Z Learning Objective: 5.eleven Describe how stereodiscriptors are assigned for certain trisubstituted and tetrasubstituted alkenes Difficulty: Medium 137. Is the following alkene E, Z, or neither? Answer: Due east Learning Objective: five.11 Draw how stereodiscriptors are assigned for certain trisubstituted and tetrasubstituted alkenes Difficulty: Medium 138. Is the following alkene E, Z, or neither? Answer: Due east Learning Objective: 5.11 Describe how stereodiscriptors are assigned for sure trisubstituted and tetrasubstituted alkenes Difficulty: Medium 139. Is the post-obit alkene Eastward, Z, or neither? If you are looking for the total examination banking concern for Klein 3e or others, email us at [email protected] for more than details. Thanks. Answer: Z Learning Objective: 5.11 Draw how stereodiscriptors are assigned for sure trisubstituted and tetrasubstituted alkenes Difficulty: Medium 140. Shown beneath is the structure of Crestor® (rosuvastatin), a medication used to reduce cholesterol. Is the highlighted alkene of rosuvastatin Due east, Z, or neither? Answer: E Learning Objective: 5.1 Compare constitutional isomers and stereoisomers, including an explanation of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Medium 141. Shown below is the structure of Singulair® (montelukast), a medication used to manage athsma. Is the alkene of montelukast E, Z, or neither? Answer: E If yous are looking for the full test banking company for Klein 3e or others, email us at [email protected] for more details. Thank you. Learning Objective: 5.1 Compare constitutional isomers and stereoisomers, including an caption of how the terms cis and trans are applied to stereoisomeric alkenes and disubstituted cycloalkanes Difficulty: Medium
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