Chapter 21: 3P (page 817)
Give the IUPAC name for each aldehyde.
a.
b.
c
Short Answer
a. 4,4-dimethylpentanal
b. 2,5,6-trimethyloctanal
c. 3,3-dichlorocyclobutanecarbaldehyde
Chapter 21: 3P (page 817)
Give the IUPAC name for each aldehyde.
a.
b.
c
a. 4,4-dimethylpentanal
b. 2,5,6-trimethyloctanal
c. 3,3-dichlorocyclobutanecarbaldehyde
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Get started for freeAn unknown compound D exhibits a strong absorption in its IR spectrum at 1692 cm-1 . The mass spectrum of D shows a molecular ion at m/z = 150 and a base peak at 121. The 1H- NMR spectrum of D is shown below. What is the structure of D?
Devise a synthesis of each compound from the given starting materials. You may also use organic alcohols having four or fewer carbons, and any organic or inorganic reagents
a)
b)
c)
-d-Glucose, a hemiacetal, can be converted to a mixture of acetals on treatment with in the presence of acid. Draw a stepwise mechanism for this reaction. Explain why two acetals are formed from a single starting material.
What carbonyl compound and alcohol are formed by hydrolysis of each acetal?
a.
b.
c.
Reaction of 5,5-dimethoxypentan-2-one with methylmagnesium iodide followed by treatment with aqueous acid forms cyclic hemiacetal Y. Draw a stepwise mechanism that illustrates how Y is formed
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