The 200 MHz ¹H NMR spectrum of 2-cyanopent-2-ene (shown) has four distinctive resonances: 8 5.3 (1H, singlet), 2.1 (2H, quartet), 1.9 (3H, singlet), 1.0 (3H, triplet). Assign each resonance to the structure. Assign the resonanses by dragging the appropriate labels to their respective targets. 5.3 1H singlet 2.1 2H quartet 1.9 3H singlet 1.0 3H triplet H3C. NC 25 CH₂CH3 H Reset Help

Chemistry
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Chapter1: Chemical Foundations
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The 200 MHz ¹ H NMR spectrum of 2-cyanopent-2-ene (shown) has four distinctive resonances: 65.3 (1H, singlet), 2.1 (2H, quartet), 1.9 (3H, singlet), 1.0 (3H, triplet). Assign each
resonance to the structure.
Assign the resonanses by dragging the appropriate labels to their respective targets.
5.3
1H
singlet
2.1
2H
quartet
1.9
3H
singlet
1.0
3H
triplet
H3C
NC
C=
2.5
CH₂CH3
H
Reset
Help
Transcribed Image Text:The 200 MHz ¹ H NMR spectrum of 2-cyanopent-2-ene (shown) has four distinctive resonances: 65.3 (1H, singlet), 2.1 (2H, quartet), 1.9 (3H, singlet), 1.0 (3H, triplet). Assign each resonance to the structure. Assign the resonanses by dragging the appropriate labels to their respective targets. 5.3 1H singlet 2.1 2H quartet 1.9 3H singlet 1.0 3H triplet H3C NC C= 2.5 CH₂CH3 H Reset Help
The 200- MHz ¹H NMR spectrum of 2-propanal (shown) has three distinctive resonances: 89.5 (1H, singlet), 2.2 (2H, quartet), 1.0 (3H, triplet)
Part A
Assign each resonance to the structure.
2.2
2H
q
9.5
1.H
S
1.0
3H
H
O
CH₂CH3
Reset
Transcribed Image Text:The 200- MHz ¹H NMR spectrum of 2-propanal (shown) has three distinctive resonances: 89.5 (1H, singlet), 2.2 (2H, quartet), 1.0 (3H, triplet) Part A Assign each resonance to the structure. 2.2 2H q 9.5 1.H S 1.0 3H H O CH₂CH3 Reset
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