EBK CHEMISTRY
13th Edition
ISBN: 9780134564630
Author: Timberlake
Publisher: YUZU
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Textbook Question
Chapter 11.2, Problem 11.7PP
Give the IUPAC name for each of the following
a.
b. CH— CH3 c. d. .
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Chances
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11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4
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a) (6pts) How many unique mono-chlorinated products can be formed and what are the
structures for the thermodynamically and statistically favored products?
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Number of Unique
Mono-Chlorinated Products
Thermodynamically
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Statistically
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b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the
formation of the thermodynamically favored product. Only draw the p-1 step. You do
not need to include lone pairs of electrons. No enthalpy calculation necessary
H
H-Cl
Chapter 11 Solutions
EBK CHEMISTRY
Ch. 11.1 - Identify each of the following as a formula of an...Ch. 11.1 - Identify each of the following as a formula of an...Ch. 11.1 - Identify each of the following properties as more...Ch. 11.1 - Identify each of the following properties as more...Ch. 11.1 - Prob. 11.5PPCh. 11.1 - Prob. 11.6PPCh. 11.2 - Give the IUPAC name for each of the following...Ch. 11.2 - Give the IUPAC name for each of the following...Ch. 11.2 - Draw the condensed structural formula for alkanes...Ch. 11.2 - Draw the condensed structural formula for alkanes...
Ch. 11.3 - Indicate whether each of the following pairs...Ch. 11.3 - Indicate whether each of the following pairs...Ch. 11.3 - Give the IUPAC name for each of the following a....Ch. 11.3 - Give the TUPAC name for each of the following: a....Ch. 11.3 - Draw the condensed structural formula for each of...Ch. 11.3 - Draw the condensed structural formula for each of...Ch. 11.3 - Draw the line-angle formula for each of the...Ch. 11.3 - Prob. 11.18PPCh. 11.4 - Heptane, used as a solvent for rubber cement, has...Ch. 11.4 - Nonane has a density of 0.79 g/mL and boils at 151...Ch. 11.4 - Write the balanced chemical equation for the...Ch. 11.4 - Write the balanced chemical equation for the...Ch. 11.5 - Identify the following as alkanes, alkenes,...Ch. 11.5 - Identify the following as alkanes, alkenes,...Ch. 11.5 - Give the IUPAC name for each of the following: a....Ch. 11.5 - Give the IUPAC name for each of the following: a....Ch. 11.5 - Draw the condensed structural formula, or...Ch. 11.5 - Prob. 11.28PPCh. 11.6 - Give the IUPAC name for each of the following,...Ch. 11.6 - Give the IUPAC name for each of the following,...Ch. 11.6 - Draw the condensed structural formula for each of...Ch. 11.6 - Prob. 11.32PPCh. 11.7 - Draw the structural formula for the product in...Ch. 11.7 - Draw the structural formula for the product in...Ch. 11.8 - Give the IUPAC name for each of the following: a....Ch. 11.8 - Give the IUPAC name for each of the following: a....Ch. 11.8 - Draw the line-angle formula for each of the...Ch. 11.8 - Draw the line-angle formula for each of the...Ch. 11.8 - Write the balanced chemical equation for the...Ch. 11.8 - Write the balanced chemical equation for the...Ch. 11 - Prob. 11.41UTCCh. 11 - Prob. 11.42UTCCh. 11 - Prob. 11.43UTCCh. 11 - Prob. 11.44UTCCh. 11 - Convert each of the following line-angle formulas...Ch. 11 - Convert each of the following line-angle formulas...Ch. 11 - Give the IUPAC name for each of the following:...Ch. 11 - Give the IUPAC name for each of the following:...Ch. 11 - Give the IUPAC name (including cis or trans, if...Ch. 11 - Give the LUPAC name (including cis or trans, if...Ch. 11 - Prob. 11.51APPCh. 11 - Prob. 11.52APPCh. 11 - Name each of the following aromatic compounds:...Ch. 11 - Prob. 11.54APPCh. 11 - Draw the condensed structural or line-angle...Ch. 11 - Draw the condensed structural or line-angle...Ch. 11 - Draw the cis and trans isomers for each of the...Ch. 11 - Draw the cis and trans isomers for each of the...Ch. 11 - Prob. 11.59APPCh. 11 - Draw the line-angle formula for each of the...Ch. 11 - Write a balanced chemical equation for the...Ch. 11 - Write a balanced chemical equation for the...Ch. 11 - Give the name for the product from the...Ch. 11 - Give the name for the product from the...Ch. 11 - Draw the condensed structural or line-angle...Ch. 11 - Draw the condensed structural or line-angle...Ch. 11 - Prob. 11.67CPCh. 11 - Prob. 11.68CPCh. 11 - Prob. 11.69CPCh. 11 - Prob. 11.70CPCh. 11 - Prob. 11.71CPCh. 11 - Prob. 11.72CPCh. 11 - Prob. 11.73CPCh. 11 - Margarines are produced from the hydrogenation of...
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- What is the lone pair or charge that surrounds the nitrogen here to give it that negative charge?arrow_forwardLast Name, Firs Statifically more chances to abstract one of these 6H 11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4 • 6H total $ 4th total 21 total 4H total ZH 2H Statistical H < 3°C-H werkst - product bund abstraction here leads to the mo favored a) (6pts) How many unique mono-chlorinated products can be formed and what are the structures for the thermodynamically and statistically favored products? Proclict 6 Number of Unique Mono-Chlorinated Products f Thermodynamically Favored Product Statistically Favored Product b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the formation of the thermodynamically favored product. Only draw the p-1 step. You do not need to include lone pairs of electrons. No enthalpy calculation necessary 'H H-Cl Waterfoxarrow_forward2. (a) Many main group oxides form acidic solutions when added to water. For example solid tetraphosphorous decaoxide reacts with water to produce phosphoric acid. Write a balanced chemical equation for this reaction. (b) Calcium phosphate reacts with silicon dioxide and carbon graphite at elevated temperatures to produce white phosphorous (P4) as a gas along with calcium silicate (Silcate ion is SiO3²-) and carbon monoxide. Write a balanced chemical equation for this reaction.arrow_forward
- this is an organic chemistry question please answer accordindly!! please post the solution in your hand writing not an AI generated answer please draw the figures and structures if needed to support your explanation hand drawn only!!!! answer the question in a very simple and straight forward manner thanks!!!!! im reposting this please solve all parts and draw it not just word explanations!!arrow_forward2B: The retrosynthetic cut below provides two options for a Suzuki coupling, provide the identities of A, B, C and D then identify which pairing is better and justify your choice. O₂N. Retro-Suzuki NO2 MeO OMe A + B OR C + Darrow_forwardthis is an organic chemistry question please answer accordindly!! please post the solution in your hand writing not an AI generated answer please draw the figures and structures if needed to support your explanation hand drawn only!!!! answer the question in a very simple and straight forward manner thanks!!!!! im reposting this please solve all parts and draw it not just word explanations!!arrow_forward
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