Compound W Has the Molecular Formula C 11 H 17 N$\delta$ 10 Quartet$\delta$ 25 Singlet

The Answer of Compound W Has the Molecular Formula C 11 H 17 N$\delta$ 10 Quartet$\delta$ 25 Singlet

Compound W Has the Molecular Formula C 11 H 17 N$\delta$ 10 Quartet$\delta$ 25 Singlet

The Answer of Compound W Has the Molecular Formula C 11 H 17 N$\delta$ 10 Quartet$\delta$ 25 Singlet

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Compound W Has the Molecular Formula C₁₁H₁₇N $\delta$ 10
Quartet $\delta$ 25
Singlet

Question 179

Multiple Choice

Compound W has the molecular formula C₁₁H₁₇N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The ¹H NMR spectrum of W consists of: triplet, $\delta$ 1.0
Quartet, $\delta$ 2.5
Singlet, $\delta$ 3.6 (2H)
Multiplet, $\delta$ 7.3 (5H)
The most likely structure for W is:

A) $Compound W has the molecular formula C11H17N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The 1H NMR spectrum of W consists of: triplet, \delta 1.0 Quartet, \delta 2.5 Singlet, \delta 3.6 (2H) Multiplet, \delta 7.3 (5H) The most likely structure for W is: A) B) C) D) E)$
B) $Compound W has the molecular formula C11H17N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The 1H NMR spectrum of W consists of: triplet, \delta 1.0 Quartet, \delta 2.5 Singlet, \delta 3.6 (2H) Multiplet, \delta 7.3 (5H) The most likely structure for W is: A) B) C) D) E)$
C) $Compound W has the molecular formula C11H17N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The 1H NMR spectrum of W consists of: triplet, \delta 1.0 Quartet, \delta 2.5 Singlet, \delta 3.6 (2H) Multiplet, \delta 7.3 (5H) The most likely structure for W is: A) B) C) D) E)$
D) $Compound W has the molecular formula C11H17N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The 1H NMR spectrum of W consists of: triplet, \delta 1.0 Quartet, \delta 2.5 Singlet, \delta 3.6 (2H) Multiplet, \delta 7.3 (5H) The most likely structure for W is: A) B) C) D) E)$
E) $Compound W has the molecular formula C11H17N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The 1H NMR spectrum of W consists of: triplet, \delta 1.0 Quartet, \delta 2.5 Singlet, \delta 3.6 (2H) Multiplet, \delta 7.3 (5H) The most likely structure for W is: A) B) C) D) E)$

Compound W Has the Molecular Formula C11H17N δ\deltaδ 10 Quartet δ\deltaδ 25 Singlet

Multiple Choice

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Compound W Has the Molecular Formula C₁₁H₁₇N $\delta$ 10
Quartet $\delta$ 25
Singlet

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