COOHCOOHCOOHCOOHCOOH--CH3H3C-ICICH3H>CICH2OHNH2NH2NH2NH2NH2CATBATMATRATPAT1. An optically inactive compoundAnswer:2. An R-enantiomerAnswer:3. A Flying-wedge representation of BATAnswer:

Answered: Image /qna-images/answer/c6c507c3-3c94-4c7d-9036-e3560e5ead0c.jpg

Answered: COOH CCH3 COOH COOH COOH COOH H- CH3…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter5: Stereochemistry At Tetrahedral Centers

Section5.SE: Something Extra

Problem 74AP: cis-1,2-Dimethylcyclohexane is optically inactive even though it has two chirality centers. Explain.

See similar textbooks

Similar questions

For the following molecules: a. How many stereogenic centers are present? b. How many stereoisomers are possible for these molecules?
Indicate the relationship between each pair. Choose from: configurational stereoisomers,conformers, constitutional isomers, or different formulas (Each term is used at least twice.)
Lithocholic acid is an Aâ€“B cis steroid found in human bile. Draw lithocholic acid showing chair conformations, as in Figure 27-11, and tell whether the hydroxyl group at C3 is axial or equatorial.
a model of cyclohexane in a chair conformation, and explain why the names “axial” and“equatorial’ are appropriate.
Using molecular models as well as structural drawings, explain why trans-decalin is rigid and cannot ring-flip whereas cis-decalin can easily ring-flip.
cis-1,2-Dimethylcyclohexane is optically inactive even though it has two chirality centers. Explain.
Draw all possible configurational stereoisomers for the given molecule below. Designate the R/S on the stereogenic centers and E/Z on the C=C
How is compound A related to compounds B–E? Choose fromenantiomers, diastereomers, constitutional isomers, or identicalmolecules.
Rank the following groups in order of decreasing priority. −CH=CH2, −CH3, −C≡CH, −H
Optical active compound 1-chloro-3-methylcyclopentane was reacting withpotassium t-butoxide in t-butanol. Two alkene products were obtained. Themain product was optically active, and the secondary product was notoptically active. What are the two products?
pls show the the isomers of butane-2,3-diol. Which pairs are enantiomers? diastereomers? mesomers? pls explain why for each
Construct models of 1,2-dibromocyclopentaneand draw all the possible stereoisomers. Label each chirality centre with an*,andan Ror S. Indicate clearly which pairs are relatedasenantiomers and which as diastereoisomersor meso.

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry: A Guided Inquiry

Chemistry

ISBN:

9780618974122

Author:

Andrei Straumanis

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

COOH CCH3 COOH COOH COOH COOH H- CH3 H3C- H C CH2OH NH2 NH2 NH2 NH2 NH2 CAT BAT MAT RAT PAT 1. An optically inactive compound Answer: 2. An R-enantiomer Answer: 3. A Flying-wedge representation of BAT Answer: