lost on this guy as wellBe sure to answer all parts.Determine a stepwise mechanism for the following reaction that illustrates why two substitutionproducts are formed. Explain why 1-bromohex-2-ene reacts rapidly with a wide ph Memeunder Sx1 reaction conditions, even though it is a 1° alkyl halide.1-bromohex-2-eneCH₂OHPart 1:The first step in the reaction proceeds according to which mechanism?CH₂CH₂CH₂CH=CHCH₂CH₂CH₂CH₂CH=CHCH₂ + CH₂OHPart 2 out of 5Draw the missing resonance contributor.Check my workOCH₁CH₂CH₂CH₂CH=CH-CH₂ + BrCH₂CH₂CH₂CH=CHCH₂CHOCH₂edit structure...Next part+HBr

Given is organic reaction.Given is nucleophilic substitution reaction.In first step we get…

Answered: Part 2 out of 5 Draw the missing…

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Part 2 out of 5 Draw the missing resonance contributor. CH₂CH₂CH.CH=CHCH₂ CH₂CH₂CH₂CH=CH-CH₂ + Br Br Br

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 8E

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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

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lost on this guy as well
Be sure to answer all parts.
Determine a stepwise mechanism for the following reaction that illustrates why two substitution
products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a wide ph Meme
under Sx1 reaction conditions, even though it is a 1° alkyl halide.
1-bromohex-2-ene
CH₂OH
Part 1:
The first step in the reaction proceeds according to which mechanism?
CH₂CH₂CH₂CH=CHCH₂
CH₂CH₂CH₂CH=CHCH₂ + CH₂OH
Part 2 out of 5
Draw the missing resonance contributor.
Check my work
OCH₁
CH₂CH₂CH₂CH=CH-CH₂ + Br
CH₂CH₂CH₂CH=CHCH₂
CH
OCH₂
edit structure...
Next part
+HBr

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