4. 3-ethylcyclohexanone is being reacted with 1-propylmagnesium bromide (Grignard reagent) in the first step followed by reaction with water in the second step. The electron pair on the carbon ionically bonded to the magnesium reacts with the electrophillic ketone carbon attached to the oxygen. This results in breaking the pi-bond between the carbon and oxygen giving the oxygen an additional lone-pair and a negative charge. The negatively charged oxygen is ionically bonded to the magnesium bromide. In the next step, one of the electron pairs on the negatively charged oxygen abstracts a hydrogen from the water. The resulting products are a secondary alcohol and magnesium ionically bonded to a bromide and hydroxide.

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4. 3-ethylcyclohexanone is being reacted with 1-propylmagnesium bromide (Grignard reagent)
in the first step followed by reaction with water in the second step. The electron pair on the
carbon ionically bonded to the magnesium reacts with the electrophillic ketone carbon
attached to the oxygen. This results in breaking the pi-bond between the carbon and oxygen
giving the oxygen an additional lone-pair and a negative charge. The negatively charged oxygen
is ionically bonded to the magnesium bromide. In the next step, one of the electron pairs on the
negatively charged oxygen abstracts a hydrogen from the water. The resulting products are a
secondary alcohol and magnesium ionically bonded to a bromide and hydroxide.
Transcribed Image Text:4. 3-ethylcyclohexanone is being reacted with 1-propylmagnesium bromide (Grignard reagent) in the first step followed by reaction with water in the second step. The electron pair on the carbon ionically bonded to the magnesium reacts with the electrophillic ketone carbon attached to the oxygen. This results in breaking the pi-bond between the carbon and oxygen giving the oxygen an additional lone-pair and a negative charge. The negatively charged oxygen is ionically bonded to the magnesium bromide. In the next step, one of the electron pairs on the negatively charged oxygen abstracts a hydrogen from the water. The resulting products are a secondary alcohol and magnesium ionically bonded to a bromide and hydroxide.
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