I'm confused about the mechanism and thus cannot decide which alkene would be the product. Reaction with primary and secondary alkyl halides gives alkanes. What about this case?

  • $\begingroup$ Hello and welcome to Chemistry.SE. If you have questions about the site you can always visit the help center. Your question appears to be of the homework type that falls under the guidelines described here. The bottom line is that in order to get guidance on this type of problem, you must show all the work and effort that you can towards solving it yourself first. For example, you could write out a mechanism and explain what the different products could be. $\endgroup$ – airhuff Mar 16 '17 at 7:26
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    $\begingroup$ 3rd degree alkyl halides undergo elimination hence give alkenes as product unlike 2nd and 1st degree alkyl halides $\endgroup$ – Nitro phenol Mar 16 '17 at 8:35
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    $\begingroup$ Note that the correct wording is primary, secondary, and tertiary. The use of $1^\circ$, $2^\circ$, and $3^\circ$ is a shorthand for that - it is not a shorthand for "first-degree", "second-degree", or "third-degree". $\endgroup$ – orthocresol Mar 16 '17 at 12:48

The reaction is E1 due to the formation of most stable tertiary carbocation, as such the double bond will be on the most substited side to give most substituted alkene as a major product.


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