ORGANIC CHEMISTRY
9th Edition
ISBN: 9780134645704
Author: WADE AND SIMEK
Publisher: PEARSON
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Chapter 16.2, Problem 16.2P
(a)
Interpretation Introduction
Interpretation:
The value of
Concept introduction:
The amount of heat released during the hydrogenation of an alkene is known as heat of hydrogenation. It is exothermic in nature and is used for comparing the stability of different types of
(b)
Interpretation Introduction
Interpretation:
The value of
Concept introduction:
The amount of heat released during the hydrogenation of an alkene is known as heat of hydrogenation. It is exothermic in nature and is used for comparing the stability of different types of alkenes.
(c)
Interpretation Introduction
Interpretation:
The value of
Concept introduction:
The amount of heat released during the hydrogenation of an alkene is known as heat of hydrogenation. It is exothermic in nature and is used for comparing the stability of different types of alkenes.
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7)
8)
FCI II
-C-C-C=C-C
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Br Br
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-C=C-Br
-CEC-C-C-
10)
11)
F Br
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12)
Br
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13)
14)
15)
CH3CHFCHFC=CH
C(OH)Br2CHF(CH2)4CH2CH3
CH3(CH2)3CH=CH(CH2)2CH3
Name
1) 3-fluoro, 1-butene
2) 2-heptene
2,3-difluoro-
1-pentene
4) 6-iodo,4-methyl-
2-decyne
5) 4,4-dibromo-
1,2-butandiol
Complete structural formula
F
-C=C-C-C-
Line formula
Condensed structural formula
N
F
CH2=CHCHFCH3
1.
Part 1: Naming Organic Compounds
он
H₁C-C-CH3
CH3
Br
CI CI
2. Br-CH-CH-CH₂
H₂C-CH-C= -CH-CH2-CH3
3.
HC-CH-CH-C-OH
5. H₂C-CH-CH₂-OH
7.
OH
4.
CH
CH₂-CH₂
6.
сно
CH-CH-CH-CH₂-CH₂
H₁₂C-CH-CH-CH-CH₁₂-CH₁₂
8.
OH
Chapter 16 Solutions
ORGANIC CHEMISTRY
Ch. 16.2 - Prob. 16.1PCh. 16.2 - Prob. 16.2PCh. 16.2 - a. Draw the resonance forms of benzene,...Ch. 16.2 - Show the product of the Diels-Alder dimerization...Ch. 16.4 - Prob. 16.5PCh. 16.6 - Make a model of cyclooctatetraene in the tub...Ch. 16.6 - Prob. 16.7PCh. 16.6 - Prob. 16.8PCh. 16.7 - Prob. 16.9PCh. 16.8A - a. Draw the molecular orbitals for the...
Ch. 16.8A - Repeat Problem16-10 for the cyclopentadienyl ions....Ch. 16.8C - Explain why each compound or ion should be...Ch. 16.8C - The following hydrocarbon has an unusually large...Ch. 16.8C - Prob. 16.14PCh. 16.8C - Prob. 16.15PCh. 16.9B - Prob. 16.16PCh. 16.9C - Show which of the nitrogen atoms in purine are...Ch. 16.9C - The proton NMR spectrum of 2-pyridone gives the...Ch. 16.9D - Prob. 16.19PCh. 16.9D - Prob. 16.20PCh. 16.10 - Prob. 16.21PCh. 16.12 - Ciprofloxacin is a member of the fluoroquinolone...Ch. 16.13 - Draw and name all the chlorinated benzenes having...Ch. 16.13 - Name the following compounds:Ch. 16.15 - The UV spectrum of 1-phenylprop-2-en-1-ol shows an...Ch. 16 - Prob. 16.26SPCh. 16 - Name the following compounds:Ch. 16 - Draw and name all the methyl, dimethyl, and...Ch. 16 - Four pairs of compounds are shown. In each pair,...Ch. 16 - One of the following hydrocarbons is much more...Ch. 16 - In Kekuls time cyclohexane was unknown, and there...Ch. 16 - Prob. 16.32SPCh. 16 - Azulene is a deep-blue hydrocarbon with resonance...Ch. 16 - Prob. 16.34SPCh. 16 - Prob. 16.35SPCh. 16 - Prob. 16.36SPCh. 16 - Prob. 16.37SPCh. 16 - Prob. 16.38SPCh. 16 - Prob. 16.39SPCh. 16 - Biphenyl has the following structure. a. Is...Ch. 16 - Anions of hydrocarbons are rare, and dianions of...Ch. 16 - How would you convert the following compounds to...Ch. 16 - Prob. 16.43SPCh. 16 - Prob. 16.44SPCh. 16 - A student found an old bottle labeled thymol on...Ch. 16 - Prob. 16.46SPCh. 16 - Prob. 16.47SPCh. 16 - Prob. 16.48SPCh. 16 - The proton NMR chemical shifts of the hydrogens in...Ch. 16 - Prob. 16.50SPCh. 16 - NMR has been used to probe many molecular...
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