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Write the mechanism of the reaction of phenylmethyl
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- List the products of the reaction of acetaldehyde and acetone with sodium ethoxide in ethanol.Explain it brieflyTwo reactions occur when sodium hydroxide is added to methyl salicylate. One is immediate and one only occurs with reflux over time. What type of reaction occurs immediately and with which functional group on methyl salicylate does it react? What type of reaction occurs with reflux over time and with which functional group on methyl salicylate does it react?Why is methyl salicylate so easily absorbed through the skin?
- write the mechanism for a decarboxylation and state the structural features necessary for a decarboxylation.Write chemical reaction of the epoxide preparation by reacting cis-2-pentene with a peroxycarboxylic acid. peroxycarboxylic acidWrite the mechanism for the following reactions: the reaction of acetyl chloride with water to form acetic acid the reaction of acetyl bromide with methylamine to form N-methylacetamide
- The substance provided can be prepared by a nucleophilic addition reaction between an aldehydeor ketone and nucleophile. Identify the reactants from which it was prepared. If the substance is an acetal, identify the carbonyl compound and the alcohol; if it is an imine or enamine, identify the carbonyl compound and the amine.Draw the product you would expect from the reaction of benzoic acid with 3-methyl-1-butanol. p-toluenesulfonic acid is the catalyst in the reactionsMethyl benzoate was exposed to a nitration test, although it was difficult to see the formation of a fragrant yellow solution. What produced this consequence?
- Write the mechanism of the reaction of phenylmethylketone with Br2 in the presence of NaOH.3)Write the reaction mechanism by drawing the experimental setups for obtaining benzoin. 7)Write the mechanism of the reaction of phenylmethylketone with Br2 in the presence of NaOH.Give the sequence of the relative reactivities of carboxylic acid derivatives. Explain why acyl chloride can be converted into ester but ester cannot be converted into acyl chloride?