- Apr 21, 2001
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I have been reviewing over sn1 and sn2 reactions, most of which are substitution, like a leaving group leaves and a nuclophile comes in. But I came across another situation, where it was not substitution, but making and breaking of c-c bond.
For example
methyl-cyclobutene + h2 -----> methyl-cyclobutane
where the double bond of the c=c changed to c-c
anyone know why this happens in sn1 and sn2 reactions?
For example
methyl-cyclobutene + h2 -----> methyl-cyclobutane
where the double bond of the c=c changed to c-c
anyone know why this happens in sn1 and sn2 reactions?
