Write a detailed mechanism for the reaction of 4,5-dimethyl-1-pentyne with methyl lithium followed by the addition of benzophenone and then a small amount of hydrochloric acid Write a detailed mechanism for the reaction of 4,5-dimethyl-1-pentyne with an excess of bromine. Write a detailed mechanism for the reaction of toluene with bromine in the presence of aluminum (III) bromide Write a detailed mechanism for the reaction of benzaldehyde with sulfur trioxide in the presence of sulfuric acid For the following NMR problem complete the following: Determine the degrees of unsaturation 1 Draw the 'H NMR Spectrum Determine the structure of the compound (show all your groups and parts for full credit) C8H17NO2 'H NMR: 5.28(2H, s), 2.78(6H, s)), 1.55(9H, s)) For the following NMR problem complete the following: Determine the degrees of unsaturation Draw the 'H NMR Spectrum Determine the structure of the compound (show all your groups and parts for full credit) C8H9SBr 'H NMR: 7.4(5H, s), 3.2(1H, q, J = 6.4Hz), 2.3(3H, d, J = 6.6Hz) IR: 1050cm-1 Identify the unique carbon environments in the following molecules a) 4-chloro-2,5-dimethyl-2-hexene b) para-nitrobenzaldehyde c) 3,4-dimethylhexane Identify all the unique hydrogen environments in the following molecules a) 3,5-dipropyl cyclohexene b) 3-bromo-2-chloro decane c) 2-ethyl-3-propyltoluene
Write a detailed mechanism for the reaction of 4,5-dimethyl-1-pentyne with methyl lithium followed by the addition of benzophenone and then a small amount of hydrochloric acid Write a detailed mechanism for the reaction of 4,5-dimethyl-1-pentyne with an excess of bromine. Write a detailed mechanism for the reaction of toluene with bromine in the presence of aluminum (III) bromide Write a detailed mechanism for the reaction of benzaldehyde with sulfur trioxide in the presence of sulfuric acid For the following NMR problem complete the following: Determine the degrees of unsaturation 1 Draw the 'H NMR Spectrum Determine the structure of the compound (show all your groups and parts for full credit) C8H17NO2 'H NMR: 5.28(2H, s), 2.78(6H, s)), 1.55(9H, s)) For the following NMR problem complete the following: Determine the degrees of unsaturation Draw the 'H NMR Spectrum Determine the structure of the compound (show all your groups and parts for full credit) C8H9SBr 'H NMR: 7.4(5H, s), 3.2(1H, q, J = 6.4Hz), 2.3(3H, d, J = 6.6Hz) IR: 1050cm-1 Identify the unique carbon environments in the following molecules a) 4-chloro-2,5-dimethyl-2-hexene b) para-nitrobenzaldehyde c) 3,4-dimethylhexane Identify all the unique hydrogen environments in the following molecules a) 3,5-dipropyl cyclohexene b) 3-bromo-2-chloro decane c) 2-ethyl-3-propyltoluene
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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Transcribed Image Text:Write a detailed mechanism for the reaction of 4,5-dimethyl-1-pentyne with methyl lithium
followed by the addition of benzophenone and then a small amount of hydrochloric acid
Write a detailed mechanism for the reaction of 4,5-dimethyl-1-pentyne with an excess of
bromine.
Write a detailed mechanism for the reaction of toluene with bromine in the presence of
aluminum (III) bromide
Write a detailed mechanism for the reaction of benzaldehyde with sulfur trioxide in the presence
of sulfuric acid
For the following NMR problem complete the following:
Determine the degrees of unsaturation
1
Draw the 'H NMR Spectrum
Determine the structure of the compound (show all your groups and parts for full credit)
C8H17NO2
'H NMR: 5.28(2H, s), 2.78(6H, s)), 1.55(9H, s))
For the following NMR problem complete the following:
Determine the degrees of unsaturation
Draw the 'H NMR Spectrum
Determine the structure of the compound (show all your groups and parts for full credit)
C8H9SBr
'H NMR: 7.4(5H, s), 3.2(1H, q, J = 6.4Hz), 2.3(3H, d, J = 6.6Hz)
IR: 1050cm-1
Identify the unique carbon environments in the following molecules
a) 4-chloro-2,5-dimethyl-2-hexene
b) para-nitrobenzaldehyde
c) 3,4-dimethylhexane
Identify all the unique hydrogen environments in the following molecules
a) 3,5-dipropyl cyclohexene
b) 3-bromo-2-chloro decane
c) 2-ethyl-3-propyltoluene
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