Given the following heats of combustion per CH2 group within the structure, which cyclic alkane has essentially no angle strain? (Ref: long-chain Alkane = 659 kJ/mol)
A) cyclobutane = 686 kJ/mol B) cyclopentane = 664 kJ/mol C) cyclohexane = 659 kJ/mol D) cycloheptane = 662 kJ/mol E) cyclooctane = 663 kJ/mol
A) protonation of the carbonyl is followed immediately by loss of the leaving group B) loss of the leaving group is followed by rearrangement of the carbocation C) addition to the carbonyl by a nucleophile is followed by loss of the leaving group D) ester hydrolysis is followed by deprotonation E) an SN2 reaction occurs