Chapter 17: Q45E (page 567)
How would you synthesize the following alcohols, starting with benzene and other alcohols of six or fewer carbons as your only organic reagents?
(a)
(b)
(c)
(d)
Short Answer
(a)
(b)
(c)
(d)
Chapter 17: Q45E (page 567)
How would you synthesize the following alcohols, starting with benzene and other alcohols of six or fewer carbons as your only organic reagents?
(a)
(b)
(c)
(d)
(a)
(b)
(c)
(d)
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Get started for freePropose structures for alcohols that have the following NMR spectra:
(a)
(b)
A compound of unknown structure gave the following spectroscopic data:
Mass spectrum:
IR:
NMR: 1.4 (2H, quartet, J=7Hz); 1.2 (6H, singlet); 1.0 (1H, singlet); 0.9 (3H, triplet, J=7Hz)
NMR: 74, 35, 27, 25
(a) Assuming that the compound contains C and H but may or may not contain O, give three possible molecular formulas.
(b) How many protons (H) does the compound contain?
(c) What functional group(s) does the compound contain?
(d) How many carbons does the compound contain?
(e) What is the molecular formula of the compound?
(f) What is the structure of the compound?
(g) Assign peaks in the molecule’s NMR spectrum corresponding to specific protons.
Question:Which of the eight alcohols that you identified in Problem 17-38 react with in aqueous acid? Show the products you would expect from each reaction
Compound A, , is one of the basic building blocks of nature. All steriods and many other naturally occurring compounds are built from compound A. Spectroscopic analysis of A yields the following information:
IR : ;
: 1.63 (3H, singlet); 1.70 (3H, singlet); 3.83 (1H, broad singlet); 4.15 (2H, doublet, J=7 Hz); 5.70 (1H, triplet, J = 7 Hz)
Question: Give IUPAC names for the following compounds:
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