Determine a stepwise mechanism for the following reaction that illustrates why two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reaction conditions, even though it is a 1° alkyl halide. Br 1-bromohex-2-ene Part 1 out of 5 CH3OH CH₂CH₂CH₂CH The first step in the reaction proceeds according to which mechanism? CHCH₂ + CH₂OH OCH3 + Br OCH₂CH₂CH₂CH: CHCH₂ 5 Br OCH 3 + HBr

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A: The relationship between moles and mass is Mass = Mole ×Molar mass

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Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.