Chapter 21: 51P (page 817)
What hydrolysis products are formed when the following compound is treated with aqueous acid?

Short Answer

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Chapter 21: 51P (page 817)
What hydrolysis products are formed when the following compound is treated with aqueous acid?


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What starting materials are needed to prepare each alkene by a Wittig reaction? When there are two possible routes, indicate which route, if any, is preferred.
a.

b

c.

What 1° amine and carbonyl compound are needed to prepare each imine?
a.

b.

Consider the para-substituted aromatic ketones, NO2C6H4COCH2 (p-nitroacetophenone) and CH3OC6H4COCH3 (p-methoxyacetophenone).
a. Which carbonyl compound is more stable?
b. Which compound forms the higher percentage of hydrate at equilibrium?
c. Which compound exhibits a carbonyl absorption at a higher wavenumber in its IR spectrum?
Explain your reasoning in each part.
Draw the products of each reaction.
a.

b.

Draw the products of the following Wittig reactions
a.

b.

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