Chapter 18: Q42P (page 967)
Sketch the expected proton NMR spectrum of 3,3-dimethylbutanal.
Short Answer
The expected proton NMR spectrum of 3,3-dimethylbutanal is as follows:
Chapter 18: Q42P (page 967)
Sketch the expected proton NMR spectrum of 3,3-dimethylbutanal.
The expected proton NMR spectrum of 3,3-dimethylbutanal is as follows:
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(a) the acid-catalyzed hydration of chloral to form chloral hydrate.
(b) the base-catalyzed hydration of acetone to form acetone hydrate
Rank the following compounds in order of increasing amount of hydrate present at equilibrium.
Show how you would accomplish the following synthesis.
(a) Acetphenone→ acetophenone cyanohydrin
(b) Cyclopentancarbaldehyde→ 2-cyclopentyl-2-hydroxyacetic acid
(c) Hexan-1-ol →2-hydroxyheptanoic acid
In the absence of water, o-phthalaldehyde has the structure shown. Its strongest IR absorption is at 1687 cm-1;the proton NMR data are shown by the structure. In the presence of water, a new compound is formed that has a strong IR absorption around 3400 cm-1and no absorption in the C=0 region. Propose a structure of X consistent with this information and suggest how X was formed.
Which of the following compounds would give a positive Tollens test? (Remember that the Tollens test involves mild basic aqueous conditions)
(a) CH3CH2COCH3
(b) CH3CH2CHO
(c) CH3CH2CH=CHCH=CHOH
(d) CH3CH2 CH2CH(OH)OCH3
(e) CH3CH2 CH2CH(OCH3)2
(f)
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