3 CI [Review Topics] Reagents HBr HBr, H₂O₂, hv a. b. C. H₂O, H₂SO4 d. Br₂ Cl₂ H₂, Pd Br₂, H₂O Cl₂, H₂O OsO4 then NaHSO3 e. f. g. h. i. j. [References] k. 1. Hg(OAc)2, H₂O then NaBH4 BH3 then H₂O2, NaOH 03 then (CH3)2S m. n. O. p. q. r. S. t. u. V. 2 equivalents of NaNH₂ H₂, Lindlar's catalyst Na/NH3 H₂SO4, HgSO4 (sia) BH then H₂O₂, NaOH 1 equivalent of NaNH₂ NBS, hv Br₂, hv Cl₂, hv HCI Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene: Step 4: V Step 5: F Step 7: Previous Next> Save and Exit

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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2
3
5
[Review Topics]
Reagents
HBr
a.
b.
C. H₂O, H₂SO4
d.
Br₂
Cl₂
H₂, Pd
Br₂, H₂O
Cl₂, H₂O
OsO4 then NaHSO3
e.
f.
g.
h.
i.
j.
k.
I.
[References]
HBr, H₂O2, hv
Hg(OAc)2, H₂O then NaBH4
BH3 then H₂O2, NaOH
O3 then (CH3)2S
m.
n.
O.
p.
q.
r.
S.
t.
u.
V.
2 equivalents of NaNH₂
H₂, Lindlar's catalyst
Na/NH3
H₂SO4, HgSO4
(sia)2BH then H₂O₂, NaOH
1 equivalent of NaNH2
NBS, hv
Br₂, hv
Cl₂, hv
HCI
Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene:
Step 4: v
Step 5: F
Step 7:
Previous
Next
Save and Exit
Transcribed Image Text:2 3 5 [Review Topics] Reagents HBr a. b. C. H₂O, H₂SO4 d. Br₂ Cl₂ H₂, Pd Br₂, H₂O Cl₂, H₂O OsO4 then NaHSO3 e. f. g. h. i. j. k. I. [References] HBr, H₂O2, hv Hg(OAc)2, H₂O then NaBH4 BH3 then H₂O2, NaOH O3 then (CH3)2S m. n. O. p. q. r. S. t. u. V. 2 equivalents of NaNH₂ H₂, Lindlar's catalyst Na/NH3 H₂SO4, HgSO4 (sia)2BH then H₂O₂, NaOH 1 equivalent of NaNH2 NBS, hv Br₂, hv Cl₂, hv HCI Identify the reagents necessary to accomplish the following steps in the above synthesis of 3-hexanone from acetylene: Step 4: v Step 5: F Step 7: Previous Next Save and Exit
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