2. Predict the products of the follwing reactions. a) Phenol + acetic anhydride b) Phenol + acetic formic anhydride c) Aniline + phthalic anhydride

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A:

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A:

Q: why pyrazole is more basic than pyridine?

A: We have to tell why pyrazole is more basic than pyridine.

Q: how can you prepare diethyl ether from an alkyl halide and any other organic or inorganic compound?

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Q: Draw a stepwise mechanism for the following reaction.

A: Please fine below the reaction mechanism.

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Q: Please draw the products for each nucleophilic substitution reaction. If there is no product, state…

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Q: Draw a stepwise mechanism for the attached reaction.

A: In organic reactions nucleophiles attack electrophiles.

Q: Propose routes to a)propylmagnesium bromide b)propylzinc bromide c)propyllithium and d)dipropylzinc…

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Q: Draw a stepwise mechanism for the following reaction.

A: Given reaction,

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A: The product(s) formed when A is treated with given reagent.

Q: Draw a stepwise mechanism for the attached reaction

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Q: how could you convert p-nitrobenzoic acid to ethyl p-nitrobenzoate

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Q: Draw a stepwise mechanism for the following reaction. ***** CI AICI3 + HCI

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Q: Friedel-Crafts alkylations usually invariably result in a mixture of products, but Friedel…

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Q: Which of the following reagent is used for hydroboration?   a Phosphoric acid   b Tetrahydrofuran…

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Q: Lexan can also be prepared by the acid-catalyzed reaction of diphenyl carbonate with bisphenol A.…

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Q: how can we convert benzene to aniline?

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Q: 3. Draw a stepwise mechanism for the following reaction. 1) NaH 2) H₂O ·8 +

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Q: Synthetize 3-pentynal from 3-butynal using whatever organic/inorganic reagents are needed.

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Q: a) Br OH b)

A:

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Q: Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With…

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