SN1 solvolysis of 3-bromocyclohex-1-ene in ethanol gives:
There is just the one major product
The reaction is slower than that of a tertiary alkyl halide in general
Two products of decent yields are formed
None of the above
Once we evaluate the intermediate, the product becomes obvious. The only product is:
SN1 solvolysis of 4-bromopent-2-ene in ethanol gives:
For the SN1 solvolysis of 5-bromopent-2-ene in ethanol, which of the following is true?
SN1 solvolysis of 1-(bromomethyl)cyclohex-1-ene in ethanol gives: