Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Textbook Question
Chapter 6, Problem 6.45SP
Predict the products of the following SN2 reactions
- a. CH3CH2ONa+CH3CH2Cl→
c.
d. CH3(CH2)8CH2Cl+Na+-:≡CH→
e.
f. (CH3)3C—CH2CH2Br+excessNH3→
h.
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Students have asked these similar questions
Which halide is least reactive towards SN2 reactions ?
O a. tert-butyl bromide
O b. sec-butyl bromide
O c. isopropyl bromide
O d. methyl bromide
O e. cyclohexyl bromide
From the table of reagents shown below, show how you synthesize the product from the given reactant.
OCH₂CH3
OH
a. NBS, (PhCO₂)2
b. Br2, FeBr3
c. Br₂, H+
d. OH
e. NaOH(s), A
f. HNO3, H₂SO4
g. H₂ CrO4
Reagents available
h. CH3 CI, AICI,
o. CuCN
i. CH3 CH₂ Br
p. H₂O+, A
j. CH₂O, A
q. CH3 CH₂ COCI, AICI,
k. CH3COCI, AICI3
r. H₂NNH₂, OH, A
1. Mg, Et₂ O
s. H₂, Pd/C
m. CO₂ (s) then H3O+ t. H₂PO₂
n. HONO 0°C
u. Cl₂, FeCl3
(Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required
to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.)
Answer:
select reagents:
cyclopentanone
Reagents
a. C6H5CHO
b. NaOH, ethanol
c. Pyrrolidine, cat. Hj.
d. H₂C=CHCN
e. H3O+
f. LDA
g.
A) bg
EtOC(=O)CO₂Et
h.
i.
B) ka
k.
I.
m.
O:
BrCH₂CH=CH₂
NatOEt, ethanol
Br₂, H+
K+ t-BUO™
CH2(CO2Et)z
heat
C) jh
CO₂Et
D) Im
Chapter 6 Solutions
Organic Chemistry (9th Edition)
Ch. 6.1 - Classify each compound as an alkyl halide, a vinyl...Ch. 6.2 - Give the structures of the following compounds. a....Ch. 6.2 - For each of the following compounds, A. give the...Ch. 6.3E - Prob. 6.4PCh. 6.4 - Prob. 6.5PCh. 6.5A - For each pair of compounds, predict which compound...Ch. 6.5B - Prob. 6.7PCh. 6.6B - Prob. 6.8PCh. 6.6B - The light-initiated reaction of...Ch. 6.6B - Show how free-radical halogenation might be used...
Ch. 6.7 - Prob. 6.11PCh. 6.7 - Prob. 6.12PCh. 6.8 - Prob. 6.13PCh. 6.9 - Predict the major products of the following...Ch. 6.9 - Prob. 6.15PCh. 6.10A - Prob. 6.16PCh. 6.11A - When diethyl ether (CH3CH2OCH2CH3) is treated with...Ch. 6.11B - Prob. 6.18PCh. 6.11B - For each pair of compounds, state which compound...Ch. 6.12 - Prob. 6.20PCh. 6.12 - Under appropriate conditions...Ch. 6.13 - Propose an SN1 mechanism for the solvolysis of...Ch. 6.13B - Prob. 6.23PCh. 6.13B - 3-Bromocyclohexene is a secondary halide, and...Ch. 6.15 - Prob. 6.25PCh. 6.15 - Prob. 6.26PCh. 6.16 - For each reaction, give the expected substitution...Ch. 6.16 - Prob. 6.28PCh. 6.16 - Prob. 6.29PCh. 6 - Prob. 6.30SPCh. 6 - Draw the structures of the following compounds. a....Ch. 6 - Give systematic (IUPAC) names for the following...Ch. 6 - Prob. 6.33SPCh. 6 - Predict the compound in each pair that will...Ch. 6 - Prob. 6.35SPCh. 6 - Give two syntheses for (CH3)2CHOCH2CH3, and...Ch. 6 - Prob. 6.37SPCh. 6 - Prob. 6.38SPCh. 6 - Chlorocyclohexane reacts with sodium cyanide...Ch. 6 - Give the substitution products expected from...Ch. 6 - Prob. 6.41SPCh. 6 - Prob. 6.42SPCh. 6 - Two of the carbocations in Problem6-42 are prone...Ch. 6 - Prob. 6.44SPCh. 6 - Predict the products of the following SN2...Ch. 6 - Prob. 6.46SPCh. 6 - Strawberry growers have used large quantities of...Ch. 6 - A solution of pure (S)-2-iodobutane ([]=+15.90) in...Ch. 6 - Prob. 6.49SPCh. 6 - Give a mechanism to explain the two products...Ch. 6 - Prob. 6.51SPCh. 6 - Because the SN1 reaction goes through a flat...Ch. 6 - Prob. 6.53SPCh. 6 - Furfuryl chloride can undergo substitution by both...Ch. 6 - Prob. 6.55SPCh. 6 - The following reaction takes place under...Ch. 6 - Propose mechanisms to account for the observed...Ch. 6 - Prob. 6.58SPCh. 6 - Prob. 6.59SP
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