aYouTube Maps My Library Bryte Question 6 of 12 Choose the molecule that is NOTA constitutional isomer to the other compounds in this group. A) Compound 1 Compound 1 Compound 2 B) Compound 2 C) Compound 3 D) Compound 4 Compound 3 Compound 4

aYouTube Maps My Library Bryte Question 6 of 12 Choose the molecule that is NOTA constitutional isomer to the other compounds in this group. A) Compound 1 Compound 1 Compound 2 B) Compound 2 C) Compound 3 D) Compound 4 Compound 3 Compound 4

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL3: Carbon (13c) Nmr Spectroscopy

Section: Chapter Questions

Problem 14E

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Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.

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Compound 1 Br Bri НІ T ... H The correct IUPAC names are: Compound 2 H Br Br I.. H Br The compounds are diastereomers not isomeric enantiomers identical constitutional isomers Compound 1: (2R, 3R)-1,2,3-tribromobutane, Compound 2: (2S, 3R)-1,2,3-tribromobutane Compound 1: (2R, 3S)-1,2,3-tribromobutane, O Compound 1: (2R,3R)-1,2,3-tribromobutane, Compound 2: (2S,3S)-1,2,3-tribromobutane Compound 2: (2R, 3R)-1,2,3-tribromobutane O Compound 1: (2S,3S)-1,2,3-tribromobutane, Compound 2: (2R,3S)-1,2,3-tribromobutane
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As mentioned in Problem 3-53, the statin drugs, such as simvastatin (Zocor), pravastatin (Pravachol), and atorvastatin (Lipitor) are the most widely prescribed drugs in the world. (a) Are the two indicated bonds on simvastatin cis or trans? (b) What are the cis/trans relationships among the three indicated bonds on pravastatin? (c) Why cant the three indicated bonds on atorvastatin be identified as cis or trans?
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5) Use compounds X, Y and Z (shown below) to answer the following questions. H. H3C" "CH3 ОН CH3 compound X compound Y compound Z a) Is compound X classified as cis, trans or neither? b) Is compound Y classified as E, Z or neither? c) Is compound Z classified as R, S or neither? d) Are compounds X and Y constitutional isomers of each other? (YES or NO) e) Are compounds Y and Z constitutional isomers of each other? (YES or NO) f) Classify compound Y as a primary, secondary or tertiary alcohol. g) Which compound(s) is(are) chiral? h) Give the IUPAC name for compound Z, omitting the absolute configuration (R or S) designation. i) In the indicated spaces below, draw stereoisomers of compounds X, Y and Z. stereoisomer of compound X stereoisomer of compound Y stereoisomer of compound Z
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11. What is the relationship between the two structures shown? H CI a) Enantiomers d) constitution isomers a) I b) II c) III 13. What is the relationship between I and II? a) cis only H Br Br CI and a) same compound b) enantiomers c) diastereomers 12. Which of the following choices is an enantiomer of the first structure shown. CI b) trans only ¢ ¢ ¢ ¢ IV d) IV b) diastereoisomers e) same compounds I I III Br || Br CI CI 14. How many diastereoisomers are there for the compound shown? OH c) both NH a) 1 b) 2 c) 3 d) 4 e) 5 f) none of above 15. Shown below is the structure of Singulair® (montelukast), a medication used to manage asthma. Is the alkene of montelukast cis, trans, or neither? S DAQUI f) none of above Page 3 of 5 c) different compounds f) none of above 1 novidad que CO₂H d) none of these Dic Incon d) neither cis nor trans
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For each pair of structures shown, indicate hether the two species are constitutional isomers, enantiomers, diastereomers of one another, or identical molecules