Are you familiar with the term "grignard reagent"? The molecule on the left side of the arrow is one (simplified with: RMgX (R=carbonchain, X=halogene)).
The Br molecule which is attached to toluene (simplified as RX) reacts as a leaving group when RMgX attacks it.
I think chenbeier made it all clear to you yesterday. But maybe this makes it more clear.
Also a tip: If you get a question where bromocyclohexane reacts with Mg (as the reagent) it will also form the molecule on the left side of the arrow.
Are you familiar with the term "grignard reagent"? The molecule on the left side of the arrow is one (simplified with: RMgX (R=carbonchain, X=halogene)).
The Br molecule which is attached to toluene (simplified as RX) reacts as a leaving group when RMgX attacks it.
I think chenbeier made it all clear to you yesterday. But maybe this makes it more clear.
Also a tip: If you get a question where bromocyclohexane reacts with Mg (as the reagent) it will also form the molecule on the left side of the arrow.
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I'm not sure. Is it (Cyclohexylmethyl)benzene?
I'm not sure. Is it (Cyclohexylmethyl)benzene?
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The Br molecule which is attached to toluene (simplified as RX) reacts as a leaving group when RMgX attacks it.
I think chenbeier made it all clear to you yesterday. But maybe this makes it more clear.
Also a tip: If you get a question where bromocyclohexane reacts with Mg (as the reagent) it will also form the molecule on the left side of the arrow.
The Br molecule which is attached to toluene (simplified as RX) reacts as a leaving group when RMgX attacks it.
I think chenbeier made it all clear to you yesterday. But maybe this makes it more clear.
Also a tip: If you get a question where bromocyclohexane reacts with Mg (as the reagent) it will also form the molecule on the left side of the arrow.
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Only cyclo hexane or?
Only cyclo hexane or?
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