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user7951
user7951

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I figured that the first reaction just adds a bromine to the meta position but I don't know what step ii) does. The only thing I can think of is the base gets rid of the alpha hydrogen next to the carbonyl... thenThen perhaps the -venegative carbon now attacks iodine? But that seems a bit off to me.

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I figured that the first reaction just adds a bromine to the meta position but I don't know what step ii) does. The only thing I can think of is the base gets rid of the alpha hydrogen next to the carbonyl... then perhaps the -ve carbon now attacks iodine? But that seems a bit off to me.

enter image description here

I figured that the first reaction just adds a bromine to the meta position but I don't know what step ii) does. The only thing I can think of is the base gets rid of the alpha hydrogen next to the carbonyl. Then perhaps the negative carbon now attacks iodine? But that seems a bit off to me.

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orthocresol
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john clastings
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What does addition of iodine and base do this case?

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I figured that the first reaction just adds a bromine to the meta position but I don't know what step ii) does. The only thing I can think of is the base gets rid of the alpha hydrogen next to the carbonyl... then perhaps the -ve carbon now attacks iodine? But that seems a bit off to me.