The tertiary alkyl halide undergo elimination reaction to give alkenes 

In Williamson synthesis of mixed ether having a primary and a tertiary alkyl group if tertiary halide is used, then :
Held on 22 Apr 2013 · Verified 6 Jul 2026.
Rate of reaction will be slow due to slow cleavage of carbon-halogen bond.
Alkene will be the main product.
Simple ether will form instead of mixed ether.
Expected mixed ether will be formed.
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