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1. The synthesis of Grignard reagent is challenging. a) Draw the product that is expected to be formed if the Grignard reagen

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Answer #1

Ans-1(a): Benzene [C6H6]1584946641000_image.png

(b): Nucleophile

Ans-2: Nucleophile

Ans-3: "the product will have low solubility in ether" is the incorrect statement. In fact it is highly soluble in ether but low solubility in water at room temperature.

Ans-4: The extraction scheme separates the pure benzoic acid from the reaction mass. The layers are as follows:

First tube = A = Ether + B = Aq. Layer

Second Tube = ether layer (A) having most of the crude benzoic acid

Third tube = After extracting with NaOH/Water + ether the C will be ether and the D = aq,. layer having most of the benzoic acid as sodium salt in ionic form.

Fourth Tube = The ether layer is again extarcted with the aq. NaOH to get the maximum recovery of benzoic acid in the separated layer in fourth tube as E.

Fifth tube: The extracted aq. sodium salt of the benzoic acid is then acidified with aq. HCl in this tube to get the pure benzoic acid as F.

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