Skip to main content
deleted 208 characters in body; edited title
Source Link
orthocresol
  • 71.9k
  • 12
  • 249
  • 423

Why is it aqueous and ethanolic conditions for nucleophillc substitution of a cyanide ion with a benzene ring bonded to a chloromethanebenzyl chloride?

Apologies I probably could of named the benzene containing molecule better what is it?

I was doing an exam question. Where there where benzyl chloride was a chloro methyl group attached to a Benzene ring asundergoing a nucleophilic substitution with cyanide ion was nucleophillically substituting with a chloro methyl group to form a nitrile bonded to a benzene ringbenzyl cyanide.

Please can someone enlighten me as I have never seen both conditions before just one or the other. I have gooogledGoogled it but no sites talk about the conditions of nucleophilllicnucleophilic substitution with a cyanide ion in a benzene context. Does the benzene alter the conditions.

Thanks very much,

Daniel?

Why is it aqueous and ethanolic conditions for nucleophillc substitution of a cyanide ion with a benzene ring bonded to a chloromethane?

Apologies I probably could of named the benzene containing molecule better what is it?

I was doing an exam question. Where there was a chloro methyl group attached to a Benzene ring as a cyanide ion was nucleophillically substituting with a chloro methyl group to form a nitrile bonded to a benzene ring.

Please can someone enlighten me as I have never seen both conditions before just one or the other. I have gooogled it but no sites talk about the conditions of nucleophilllic substitution with a cyanide ion in a benzene context. Does the benzene alter the conditions.

Thanks very much,

Daniel

Why is it aqueous and ethanolic conditions for nucleophillc substitution of cyanide ion with benzyl chloride?

I was doing an exam question where benzyl chloride was undergoing a nucleophilic substitution with cyanide ion to form benzyl cyanide.

Please can someone enlighten me as I have never seen both conditions before just one or the other. I have Googled it but no sites talk about the conditions of nucleophilic substitution with a cyanide ion in a benzene context. Does the benzene alter the conditions?

Source Link
daniel
  • 63
  • 2
  • 4

Why is it aqueous and ethanolic conditions for nucleophillc substitution of a cyanide ion with a benzene ring bonded to a chloromethane?

Apologies I probably could of named the benzene containing molecule better what is it?

I was doing an exam question. Where there was a chloro methyl group attached to a Benzene ring as a cyanide ion was nucleophillically substituting with a chloro methyl group to form a nitrile bonded to a benzene ring.

Please can someone enlighten me as I have never seen both conditions before just one or the other. I have gooogled it but no sites talk about the conditions of nucleophilllic substitution with a cyanide ion in a benzene context. Does the benzene alter the conditions.

Thanks very much,

Daniel