How to practice Stereochemistry

Attempt a question, record the concept and assumptions, then check the available answer. Rework mistakes after revising the relevant concepts. Topic tags can overlap; review the question context.

Questions 1–10 of 33. Imported answers require independent review unless marked reviewed.

Topic practice 33 questionsPage 1 of 4

Question 12

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The correct statement about the following quaternary ammonium ion is
Diagram for Chemistry question 12

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Question 22

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The reaction(s) that give(s) meso-1,2-diphenylethane-1,2-diol as the major product is(are)
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Question 23

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In the ¹H NMR spectrum of compound X, the coupling constant (Jₐᵦ) between Hₐ and Hᵦ is 3 Hz. The amino alcohol(s) that give(s) X on reaction with methyl iodide followed by heating is(are)
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Question 29

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The difference in the number of gauche interactions present in diaxial and diequatorial chair conformations of trans-1,2-dimethylcyclohexane is _____ (in integer).

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Question 33

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The specific rotation of enantiomerically pure (S)-2-butanol is +14°. The specific rotation of enantiomeric mixture of 2-butanol obtained from an asymmetric reduction of 2-butanone is found to be +7°. The percentage of (R)-2-butanol present in the reaction mixture is ______ (in integer).

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Question 44

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In the following asymmetric transformation, the key aldol reaction involves the attack of
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Question 55

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For the following reaction, the possible product(s) is/are
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Question 15

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Among the following, the chiral compound is
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Question 26

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The correct statement(s) for decalin is (are)
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Question 41

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Fischer presentation of D-(-)-fructose is given below.
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The correct structure of

-L-(+)-fructofuranose is
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