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explanation please

thanx

2007-03-12 02:51:05 · 3 answers · asked by Tommy 2 in Science & Mathematics Chemistry

3 answers

You use the Stephen aldehyde synthesis:

R-CN + HCl + SnCl2 → [R-CH=NH2]+Cl- + H2O → R-CHO

The nitrile forms an iminium salt with tin chloride which is then hydrolysed to the aldehyde.

2007-03-12 02:59:28 · answer #1 · answered by Dr Dave P 7 · 0 0

Stephen aldehyde synthesis, a named reaction in chemistry, invented by Henry Stephen (OBE/MBE). This reaction involves the preparation of aldehydes (R-CHO) from nitriles (R-CN) using Tin(II) chloride (SnCl2), hydrochloric acid (HCl) and quenching the resulting iminium salt ([R-CH=NH2]+Cl-) with water (H2O) [1] .

OR

you can use the strecker synthesis, from a nitrile you oxydize it to a COOH with OH- and H2O.
Then you reduce the acid to aldehyde.

2007-03-12 10:17:41 · answer #2 · answered by scientific_boy3434 5 · 0 0

Sn/HCl or LiAlH(O-t-Bu)3

will do the conversion of the nitrile to the hydride

do you need the mechanism? Otherwise list it as an redox reaction.

2007-03-12 10:27:19 · answer #3 · answered by jeepinebay 1 · 0 0

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