Which of the following is the intermediate for halogenation conditions? An enola

Question

Which of the following is the intermediate for halogenation conditions? An enolate An enolate A tautomer An epimer The reaction below is a direct enolatc alkylation It has been found that only works well with unhindered methyl and 1degree alkyl halides. Pick the statement that best explains this observation The nucleophilic enolate requires a reaction center that has a positive charge. Hindered alkyl halides do not undergo SnI reactions Hindered alkyl halides do not undergo S_N2 reactions Methyl and 1degree alkyl halides can form carbocations that can readily react with the nucleophilic enolate. Which is the thermodynamic enolate of 2-methylcyclohexanone? I II III IV Which of the following statements about Aldol reactions with either aldehydes or ketones is true? Equilibrium favors the products with aldehydes, equilibrium favors the starting materials with ketones. Equilibrium favors the starting materials with aldehydes; equilibrium favors the products with ketones. Equilibrium favors the products with both aldehydes and ketones. Equilibrium favors the starting materials with both aldehydes and ketones. What reaction type is an Aldol reaction? nucleophilic substitution electrophilic substitution electrophilic addition nucleophilic addition

Explanation / Answer

6)A

8)C

9)A

10)D

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