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- Provide all possible products formed in the given reaction Draw the products formed when each ether is treated with two equivalents of HBr.An acetal can be hydrolyzed by treatment with aqueous acid.Draw the tautomer of this enol. Include all lone pairs. Ignore inorganic byproducts. :OH: :0: H3O+ Draw Tautomer
- Why is it not advisable to use aqueous hydrochloric acid in a Grignard reaction of a ketone? A) The Grignard reagent will react with the acid and cannot react with the ketone. B) The ketone will be protonated and will become unreactive. C) The ketone will form an unreactive enol. D) The Grignard reagent won't dissolve in aqueous solutionsTo prepare an ether from an alkyl halide by a nucleophilic substitution reaction, what are the two types of nucleophiles that can be used?Do dicarbonyls or ketones react faster? Explain why
- What are the major organic products of each reaction.According to Le Chatelier's Principle, acetal product formation tends to INCREASE (rather than decrease) when more alcohol is added to the reaction mixture. True or False?Compare aldehydes and ketones as to (Use acetaldehyde and acetone as examples). 1. Reaction with Tollen’s reagent 2. Reaction with Fehling’s reagent 3. Reaction with dilute NaOH
- Explain why pentane-2,4-dione forms two different alkylation products (Aor B) when the number of equivalents of base is increased from one totwo.Rank the following in order of decreasing solubility in benzene. gallic acid ethyl benzene resorcinolAcetal formation must be catalyzed by an acid. Explain why it cannot be catalyzed by CH3O-.