Define alpha-iodobutyric acid

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Reference no: EM13178279

1. Draw the following compounds:

a. alpha-iodobutyric acid

b. phenoxy propionate

c. beta-ketoadipic acid

2. Name this compound

CH3CHCH2CH3

CH3CNCH3

3. Fill in the steps to complete the following synthesis. You may need more than one reaction to complete each transformation.

a. Benzene -> meta-ethylnitrobenzene Steps:

b. Meta-ethylnitrobenzene -> meta-bromoethylbenzene Steps:

4. Draw products A through E for the following series of reactions. If both ortho and para product would form, continue on only with the para product, but mention that ortho would also be a product.

Chlorobenzene + HNO3/H2SO4 -> Product A

Product A + OH-, heat -> Product B

Product B + Sn, HCl, followed by hydroxide -> Product C

Product C + NaNO2/HCl, zero degrees celcius -> Product D

Product D + HBF4 -> Product E

5. Show the steps needed to synthesize para-bromobenzoic acid from toluene.

Reference no: EM13178279

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