camparing vanious alkyl halidesreactivity toward SN1 reactions usingwater as a nucleopnileEntry # Alko| halide K(x101min")0.2231 t 0.0041Eq(kcsI)COHS CH 2 C1Cetts CH2BrcoHs CHCI 2Ce Hs CHCIBrCuts CCI3CoHs CC12 Br A 212214)21.22.5684I 0.08519.12.214 E 0.03723.331.08 1 0.19110.5 0.9421.920.519.2reaction was dame in 50%. aqueOUSacetune at 30°Creactionn scherrefur entry #1H2O->acetane d) what isthe full maartien mechanismof Entry # reaction.e) Aranas unat is the trond obserredin the study based on the rate of reaction.

Answered: Image /qna-images/answer/656e4672-55c6-4f3a-9ee2-336fb3a39084.jpg

Answered: d) what is tre full maartion mechanism…

d) what is tre full maartion mechanism Of Entry #4 reaction. e) Adraias unat is tre trend observed in the study based on the rate of reaction.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

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camparing vanious alkyl halides
reactivity toward SN1 reactions using
water as a nucleopnile
Entry # Alko| halide K(x101min")
0.2231 t 0.0041
Eq(kcsI)
COHS CH 2 C1
Cetts CH2Br
coHs CHCI 2
Ce Hs CHCIBr
Cuts CCI3
CoHs CC12 Br A 212214)
21.2
2.
5684I 0.085
19.1
2.214 E 0.037
23.3
31.08 1 0.19
110.5 0.9
4
21.9
20.5
19.2
reaction was dame in 50%. aqueOUS
acetune at 30°C
reaction
n scherre
fur entry #1
H2O
->
acetane

d) what isthe full maartien mechanism
of Entry # reaction.
e) Aranas unat is the trond obserred
in the study based on the rate of reaction.

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