EP ESSENTIAL ORG.CHEM.-MOD.MASTERING
3rd Edition
ISBN: 9780133858501
Author: Bruice
Publisher: PEARSON CO
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Textbook Question
Chapter 14, Problem 15P
- a. Would chlorination or bromination produce a greater yield of 2–halo–2,3–dimethylbutane?
- b. Would chlorination or bromination be a better way to make 1–halo–2,2–dimethylpropane?
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Correctly name this compound using the IUPAC naming system by sorting the
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Br
IN
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H
How is the radical intermediate for this structure formed? Can you please draw arrows from the first radical to the resonance form that would result in this product? I'm lost.
Part VI.
(a) calculate the λ max of the compound using woodward - Fieser rules.
(b) what types of electronic transitions are present in the compound?
(c) what are the prominent peaks in the IR spectrum of the compound?
Chapter 14 Solutions
EP ESSENTIAL ORG.CHEM.-MOD.MASTERING
Ch. 14.2 - Write the mechanism for the monobromination of...Ch. 14.2 - Prob. 2PCh. 14.4 - Prob. 3PCh. 14.4 - Which of the hydrogens in the structure in the...Ch. 14.4 - How many alkyl chlorides can be obtained from...Ch. 14.4 - Prob. 7PCh. 14.5 - Prob. 9PCh. 14.6 - a. Which ether is most apt to form a peroxide? b....Ch. 14.7 - Prob. 11PCh. 14 - Prob. 12P
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