Chapter 11: Q.11-50a (page 350)
Question:What products would you expect from the reaction of 1-bromopropane with each of the following?
(a) NaNH2
Short Answer
Answer
Chapter 11: Q.11-50a (page 350)
Question:What products would you expect from the reaction of 1-bromopropane with each of the following?
(a) NaNH2
Answer
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Get started for freeAmong the many examples of reactions that occur with incomplete racemization, the optically pure tosylate of 2,2-dimethyl-1-phenyl-1-propan(= 230.3) gives the corresponding acetate (= 15.3) when heated inacetic acid. If complete inversion had occurred, the optically pure acetatewould have had= 153.6. What percentage racemization and what percentageinversion occurred in this reaction?
Question: The reactions shown below are unlikely to occur as written. Tell what is wrong with each, and predict the actual product.
a.
What stereochemistry do you expect for the alkene obtained by E2 elimination of (1R, 2R)-1,2-dibromo-1,2-diphenylethane? Draw a Newman projection of the reacting conformation.
Which isomer would you expect to undergo E2 elimination faster, trans-1-bromo-4-tert-butylcyclohexane or cis-1-bromo-4-tert-butylcyclohexane? Draw each molecule in its more stable chair conformation, and explain your answer.
Rank the following substances in order of their expected reactivity:
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