What are the chemical structure of me сиз сиз (excess] following musing compocents Brz. mono substituted MAHAA 2 G3 77 excess KM 12 छाट reduction E2 Reduction (mild pond) NaBH3 CH 3 Mg Br HLOH H E3 HOW Hyle. bor. Holt aid. H3 oxymer/ demo. H2 Three compounds A, B, and C all have the formula C6H10. All three compounds rapidly decolorize bromine in CC14; all three are soluble in cold concentrated sulfuric acid. Compound A has an absorption in its IR spectrum at about 3300 cm, but compounds B and C do not. Compounds A and B both yield hexane when they are treated with excess hydrogen in the presence of a platinum catalyst. Under these conditions C absorbs only one molar equivalent of hydrogen and gives a product with the formula C6H12. When A is oxidized with hot basic potassium permanganate and the resulting solution acidified, the only organic product that can be isolated is CH3(CH2) 3CO₂H. Similar oxidation of B gives only CH3CH2CO₂H, and similar treatment of C gives only HO₂C(CH2) 4CO2H. What are the structure for A, B, and C? Starting with 2-methylpropene and using any other needed reagents, outline a synthesis of each of the following: a. (CH3)3COH b. (CH3)3CBr c. (CH3) C(OH)CH₂CI 2
What are the chemical structure of me сиз сиз (excess] following musing compocents Brz. mono substituted MAHAA 2 G3 77 excess KM 12 छाट reduction E2 Reduction (mild pond) NaBH3 CH 3 Mg Br HLOH H E3 HOW Hyle. bor. Holt aid. H3 oxymer/ demo. H2 Three compounds A, B, and C all have the formula C6H10. All three compounds rapidly decolorize bromine in CC14; all three are soluble in cold concentrated sulfuric acid. Compound A has an absorption in its IR spectrum at about 3300 cm, but compounds B and C do not. Compounds A and B both yield hexane when they are treated with excess hydrogen in the presence of a platinum catalyst. Under these conditions C absorbs only one molar equivalent of hydrogen and gives a product with the formula C6H12. When A is oxidized with hot basic potassium permanganate and the resulting solution acidified, the only organic product that can be isolated is CH3(CH2) 3CO₂H. Similar oxidation of B gives only CH3CH2CO₂H, and similar treatment of C gives only HO₂C(CH2) 4CO2H. What are the structure for A, B, and C? Starting with 2-methylpropene and using any other needed reagents, outline a synthesis of each of the following: a. (CH3)3COH b. (CH3)3CBr c. (CH3) C(OH)CH₂CI 2
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter4: Polar Bonds, Polar Reactions
Section: Chapter Questions
Problem 4E
Related questions
Question
![What are the chemical structure of me
сиз сиз
(excess]
following musing compocents
Brz.
mono substituted
MAHAA <Mglether
CH
ААА Кры
A4
のよ
Navb
H
CH3CH2Br
A
B3 Na NH₂ BB
F3
сиз енгви
некро
Teq
29.
لا
H2O, H2SO4
Hgs04
H20
79
BH3 14202
B5
E
CH3 Mg Br
B4
(KOH alchol.)
Na NHz.
Teq
Br2
если
Боября оче
2/18-20
ABY
BB
B
E
2044/48
BA
Cold.
(020804)
D2
Lindlar Cat. V
C
14504
Conc
473804
NaN Hz
CH3 Br
(H2/P-2) D3 Li/NH Du
KMnDq
(GROs) not
F2 < KMnO4
KMnO4 F
=
oxid.
#/OH
Brz
G2
KMnO4
not >
2 G3
77
excess
KM 12
छाट
reduction
E2
Reduction
(mild pond)
NaBH3
CH 3 Mg Br
HLOH
H
E3
HOW
Hyle. bor.
Holt
aid.
H3
oxymer/
demo.
H2
Three compounds A, B, and C all have the formula C6H10. All three compounds rapidly
decolorize bromine in CC14; all three are soluble in cold concentrated sulfuric acid.
Compound A has an absorption in its IR spectrum at about 3300 cm, but compounds B
and C do not. Compounds A and B both yield hexane when they are treated with excess
hydrogen in the presence of a platinum catalyst. Under these conditions C absorbs only
one molar equivalent of hydrogen and gives a product with the formula C6H12. When A is
oxidized with hot basic potassium permanganate and the resulting solution acidified, the
only organic product that can be isolated is CH3(CH2) 3CO₂H. Similar oxidation of B
gives only CH3CH2CO₂H, and similar treatment of C gives only HO₂C(CH2) 4CO2H.
What are the structure for A, B, and C?
Starting with 2-methylpropene and using any other needed reagents, outline a synthesis
of each of the following:
a. (CH3)3COH
b. (CH3)3CBr
c. (CH3) C(OH)CH₂CI
2](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F2ab948a5-8358-42f4-bb7d-05d36a9ebc0e%2Fc6fb42e5-91f4-4b3c-89ee-518f5a9c23af%2Fi06kua_processed.jpeg&w=3840&q=75)
Transcribed Image Text:What are the chemical structure of me
сиз сиз
(excess]
following musing compocents
Brz.
mono substituted
MAHAA <Mglether
CH
ААА Кры
A4
のよ
Navb
H
CH3CH2Br
A
B3 Na NH₂ BB
F3
сиз енгви
некро
Teq
29.
لا
H2O, H2SO4
Hgs04
H20
79
BH3 14202
B5
E
CH3 Mg Br
B4
(KOH alchol.)
Na NHz.
Teq
Br2
если
Боября оче
2/18-20
ABY
BB
B
E
2044/48
BA
Cold.
(020804)
D2
Lindlar Cat. V
C
14504
Conc
473804
NaN Hz
CH3 Br
(H2/P-2) D3 Li/NH Du
KMnDq
(GROs) not
F2 < KMnO4
KMnO4 F
=
oxid.
#/OH
Brz
G2
KMnO4
not >
2 G3
77
excess
KM 12
छाट
reduction
E2
Reduction
(mild pond)
NaBH3
CH 3 Mg Br
HLOH
H
E3
HOW
Hyle. bor.
Holt
aid.
H3
oxymer/
demo.
H2
Three compounds A, B, and C all have the formula C6H10. All three compounds rapidly
decolorize bromine in CC14; all three are soluble in cold concentrated sulfuric acid.
Compound A has an absorption in its IR spectrum at about 3300 cm, but compounds B
and C do not. Compounds A and B both yield hexane when they are treated with excess
hydrogen in the presence of a platinum catalyst. Under these conditions C absorbs only
one molar equivalent of hydrogen and gives a product with the formula C6H12. When A is
oxidized with hot basic potassium permanganate and the resulting solution acidified, the
only organic product that can be isolated is CH3(CH2) 3CO₂H. Similar oxidation of B
gives only CH3CH2CO₂H, and similar treatment of C gives only HO₂C(CH2) 4CO2H.
What are the structure for A, B, and C?
Starting with 2-methylpropene and using any other needed reagents, outline a synthesis
of each of the following:
a. (CH3)3COH
b. (CH3)3CBr
c. (CH3) C(OH)CH₂CI
2
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by step
Solved in 2 steps with 1 images
Recommended textbooks for you
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:
9780618974122
Author:
Andrei Straumanis
Publisher:
Cengage Learning
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:
9781305446021
Author:
Lampman
Publisher:
CENGAGE LEARNING - CONSIGNMENT
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:
9781938168390
Author:
Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:
OpenStax
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:
9780618974122
Author:
Andrei Straumanis
Publisher:
Cengage Learning
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:
9781305446021
Author:
Lampman
Publisher:
CENGAGE LEARNING - CONSIGNMENT
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:
9781938168390
Author:
Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:
OpenStax