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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Show two methods to synthesize each alkene: a one-step method using a Wittig reagent, and a two-step method that forms a carbon–carbon bond with an organometallic reagent in one of the steps.
a.

b.

What reagents are needed to convert each compound into butanal (CH3CH2CH2CHO )?
a.

b.

c.

Draw the structure of all constitutional isomers that contain a ketone and have molecular formula . Give the IUPAC name for each isomer and state how NMR spectroscopy could be used to distinguish these isomers.
Draw the products (including stereoisomers) formed when benzaldehyde (C6H5CHO) is treated with each Wittig reagent
a.

b.


Draw a stepwise mechanism for the following imine hydrolysis

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