Which one of the following aromatic compounds is the most electron rich (nucleophilic)? O bromobenzene O anisole show work. don't Otoluene Obenzene give Ai generated solution
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- Which atom in the following molecule is considered the electrophilic site, i.e. where would a nucleophile attack? O The O atom in the carbonyl (C=O) group O the Catom in the carbonly (C=O) group O Any H atom O AC atom not in the carbonyl (C=O) groupWhich of the following would be LEAST reactive for electrophilic aromatic substitution? a) CH b) Oc O a Od Ob H₂N- (၁ CH O₂H SO₂H d) CHFraw the lower and higher molecular weight
- PayalbenWhich statement(s) is(are) true concerning the rate-limiting step involving the benzene ring? CI AICI3 O aromaticity is restored aromaticity is disrupted proton transfer occurs carbocation intermediate forms O the benzene ring functions as the nucleophile the benzene ring functions as the electrophileWhich reagent is the nucleophile in the esterification reaction shown below? O || С-ОН Benzoic Acid methanol methyl benzoate benzoic acid sulfuric acid + CH₂-OH Methanol H₂SO - H₂O O || C-O-CH3 Methyl benzoate
- A Grignard reagent is made with the given bromoalkane. Draw the final product when the Grignard reagent reacts with the given compound followed by workup with H3O+. i) 1-bromo-3,3-dimethylbutane + 3-methylbutanal ---->ii) 1-bromo-3,3-dimethylbutane + butanoic acid. ---->iii) bromocyclopentane + cyclopentanone. ---->Iv) 7-bromo-4-methyl-2-heptanone (intramolecular rxn) ---->Which of the following is NOT a correct statement about the electrophilic aromatic substitution mechanism? Benzene functions as a nucleophile. Aromaticity is regained by loss of H*. Formation of a carbocation intermediate is the rate-determining step. The carbocation intermediate contains an sp° hybridized carbon in the ring. O The addition product is a frequent minor product.Like carbocations, radicals formed from compounds that contain another functional group can undergo intramolecular reactions. Draw a stepwise mechanism for the chain-propagating steps of the following intramolecular reaction.
