7. The correct structure of (1S,3R,4E)-3-amino-1-chloro-1-ethoxyhept-5-en-2-one is H2N. H2N. CI a. b. c. он CI он CI NH2 ČH2CH3 ČH2CH3 ČH2CH3 H2N OCH2CH3 CH3CH20 H. H2N OCH2CH3 H3C. H2N. CI d. e. f. H. CI H CI I NH2 8. Which regent below would effectively yield a nitrile from a benzenediazonium ion? a. NaCN b. CH3CN c. NaNH2 d. CUCN e. NH2NH2 e 9. The expected major product of the following reaction is 1. CH3CH,Li, XS CHз 2. H3O* но HO, a. C. e. "ОН b. d. f. no reaction B 10. equivalent of HOCH2CH2OH, H* protects the are more reactive than so treatment with one oldohudog kkotonog oldobude I. H. エ

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Question 8

7. The correct structure of (1S,3R,4E)-3-amino-1-chloro-1-ethoxyhept-5-en-2-one is
H2N.
H2N.
CI
a.
b.
c.
он
CI
он
CI
NH2
ČH2CH3
ČH2CH3
ČH2CH3
H2N
OCH2CH3
CH3CH20
H.
H2N
OCH2CH3
H3C.
H2N.
CI
d.
e.
f.
H.
CI
H CI
I
NH2
8. Which regent below would effectively yield a nitrile from a benzenediazonium ion?
a. NaCN
b. CH3CN
c. NaNH2
d. CUCN
e. NH2NH2
e 9. The expected major product of the following reaction is
1. CH3CH,Li, XS
CHз
2. H3O*
но
HO,
a.
C.
e.
"ОН
b.
d.
f. no reaction
B 10.
equivalent of HOCH2CH2OH, H* protects the
are more reactive than
so treatment with one
oldohudog kkotonog
oldobude
I.
H.
エ
Transcribed Image Text:7. The correct structure of (1S,3R,4E)-3-amino-1-chloro-1-ethoxyhept-5-en-2-one is H2N. H2N. CI a. b. c. он CI он CI NH2 ČH2CH3 ČH2CH3 ČH2CH3 H2N OCH2CH3 CH3CH20 H. H2N OCH2CH3 H3C. H2N. CI d. e. f. H. CI H CI I NH2 8. Which regent below would effectively yield a nitrile from a benzenediazonium ion? a. NaCN b. CH3CN c. NaNH2 d. CUCN e. NH2NH2 e 9. The expected major product of the following reaction is 1. CH3CH,Li, XS CHз 2. H3O* но HO, a. C. e. "ОН b. d. f. no reaction B 10. equivalent of HOCH2CH2OH, H* protects the are more reactive than so treatment with one oldohudog kkotonog oldobude I. H. エ
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