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In Williamson synthesis of mixed ether having a primary and a tertiary alkyl group if tertiary halide is used, then :a)Rate of reaction will be slow due to slow cleavage of carbon-halogen bond.b)Alkene will be the main product.c)Simple ether will form instead of mixed ether.d)Expected mixed ether will be formed.Correct answer is option 'B'. Can you explain this answer? for NEET 2024 is part of NEET preparation. The Question and answers have been prepared
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In Williamson synthesis of mixed ether having a primary and a tertiary alkyl group if tertiary halide is used, then :a)Rate of reaction will be slow due to slow cleavage of carbon-halogen bond.b)Alkene will be the main product.c)Simple ether will form instead of mixed ether.d)Expected mixed ether will be formed.Correct answer is option 'B'. Can you explain this answer?, a detailed solution for In Williamson synthesis of mixed ether having a primary and a tertiary alkyl group if tertiary halide is used, then :a)Rate of reaction will be slow due to slow cleavage of carbon-halogen bond.b)Alkene will be the main product.c)Simple ether will form instead of mixed ether.d)Expected mixed ether will be formed.Correct answer is option 'B'. Can you explain this answer? has been provided alongside types of In Williamson synthesis of mixed ether having a primary and a tertiary alkyl group if tertiary halide is used, then :a)Rate of reaction will be slow due to slow cleavage of carbon-halogen bond.b)Alkene will be the main product.c)Simple ether will form instead of mixed ether.d)Expected mixed ether will be formed.Correct answer is option 'B'. Can you explain this answer? theory, EduRev gives you an
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