Design three different synthesis routes to make 3-octanol, with each one including a carbon-carbonbond formation reaction, as listed, as a step in each synthesis (the reaction will not represent thefull synthesis, just part of itDirect addition to an acid chloride (to be clear, you should use two molecules, one of thembeing an acid chloride, to make an 8-carbon chain that can be converted to 3-octanol)а.b. Conjugate addition to an enoneС.Reaction between an enolate and an alkyl halide

a. Reaction between acid chloride and Gilman reagent give 3-octanone. 3-octanone is reduced to…

Design three different synthesis routes to make 3-octanol, with each one including a carbon-carbon pond formation reaction, as listed, as a step in each synthesis (the reaction will not represent the ull synthesis, just part of it a. Direct addition to an acid chloride (to be clear, you should use two molecules, one of them being an acid chloride, to make an 8-carbon chain that can be converted to 3-octanol) b. Conjugate addition to an enone C. Reaction between an enolate and an alkyl halide

Design three different synthesis routes to make 3-octanol, with each one including a carbon-carbon pond formation reaction, as listed, as a step in each synthesis (the reaction will not represent the ull synthesis, just part of it a. Direct addition to an acid chloride (to be clear, you should use two molecules, one of them being an acid chloride, to make an 8-carbon chain that can be converted to 3-octanol) b. Conjugate addition to an enone C. Reaction between an enolate and an alkyl halide

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 15CTQ

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