Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Textbook Question
Chapter 5, Problem 24PP
Practice Problem 5.24
Give names chat include (R) and (S) designations for your answers to Practice Problem 5.22.
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Students have asked these similar questions
a) Considering compounds 2a through 21, identify: ONE PAIR of geometric isomers;
TWO PAIRS of enantiomers and THREE PAIRS of identical molecules.
b)
Give the names, including the configurations, of each of the geometric isomers and
of each of the enantiomers. Draw the relevant structures in the space provided in
the Answer Booklet.
c) Sort compounds 2a, 2b, 2c, 2f and 2k in order of increasing solubility in water and
briefly justify your ordering.
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PRACTICE PROBLEM 2.2
The compounds in each part below have the same (or similar) molecular weights. Which
compound in cach part would you expect to have the higher boiling point? Explain your
answers.
(a)
OH or
(c)
OH or HO
(b) (CHN or
A factor (in addition to polarity and hydrogen bonding) that affects the melting point
of many organic compounds is the compactness and rigidity of their individual molecules.
• Molecules that are symmetrical generally have abnormally high melting points. sert-
Buryl alcohol, for example, has a much higher melting point than the other isomeric
alcohols shown here:
OH
OH
tert-Butyl alcohol
(mp 25 "C)
Butyl alcohol
(mp -00 "C)
Isobutyl alcohol sec-Butyl alcohol
(mp 108 C)
(mp-114 C)
о о
2.
Using the Roman Numerals provided, rank the following compounds in order of increasing
boilıng point. Briefly explain your answer (you should justify the position of each compound in the
ranking).
() 2,3-dimethylheptane (I) pentane (III) 2-methylbutane (IV) 2,2-dimethylpropane
Rank:
Chapter 5 Solutions
Organic Chemistry
Ch. 5 - Prob. 1PPCh. 5 - Prob. 2PPCh. 5 - Prob. 3PPCh. 5 - Prob. 4PPCh. 5 - Prob. 5PPCh. 5 - Prob. 6PPCh. 5 - Prob. 7PPCh. 5 - Practice Problem 5.8 Write three-dimensional...Ch. 5 - Prob. 9PPCh. 5 - Prob. 10PP
Ch. 5 - Practice Problem 5.11 List the substituents in...Ch. 5 - Prob. 12PPCh. 5 - Practice Problem 5.13 Tell whether the two...Ch. 5 - Prob. 14PPCh. 5 - Prob. 15PPCh. 5 - Prob. 16PPCh. 5 - Prob. 17PPCh. 5 - Prob. 18PPCh. 5 - Prob. 19PPCh. 5 - Prob. 20PPCh. 5 - Practice Problem 5.21 The following are formulas...Ch. 5 - Practice Problem 5.22 Write three-dimensional...Ch. 5 - Prob. 23PPCh. 5 - Practice Problem 5.24 Give names chat include (R)...Ch. 5 - Prob. 25PPCh. 5 - Prob. 26PPCh. 5 - Prob. 27PPCh. 5 - Prob. 28PPCh. 5 - Practice Problem 5.29 Write formulas for all of...Ch. 5 - Prob. 30PPCh. 5 - Prob. 31PPCh. 5 - Prob. 32PPCh. 5 - Prob. 33PCh. 5 - Prob. 34PCh. 5 - 5.35 Designate the (R) or (S) configuration at...Ch. 5 - Prob. 36PCh. 5 - (a) Write the structure of...Ch. 5 - Shown below are Newman projection formulas for...Ch. 5 - 5.39 Write appropriate structural formulas...Ch. 5 - Discuss whether each of the following compounds...Ch. 5 - Prob. 42PCh. 5 - Prob. 43PCh. 5 - Compound F has the molecular formula C5H8 and is...Ch. 5 - Prob. 45PCh. 5 - Prob. 46PCh. 5 - Prob. 47PCh. 5 - For the following molecule, draw its enantiomer as...Ch. 5 - 5.49 (Use models to solve this...Ch. 5 - 5.50 (Use models to solve this...Ch. 5 - (Use models co solve this problem.) Write...Ch. 5 - 5.52 Tartaric acid was an important compound in...Ch. 5 - Prob. 53PCh. 5 - Prob. 54PCh. 5 - Prob. 55PCh. 5 - Prob. 1LGPCh. 5 - Prob. 2LGPCh. 5 - Prob. 3LGP
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