
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 12.9, Problem 8P
As measured by their first-order rate constants, the compound shown (
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e two substances in each sample can interconvert. That is, each kind of molecule can turn into the other. The equilibrium constant K for each interconversion
equilibrium is shown below the sketch.
Decide whether each solution is at equilibrium.
e
8
800
K=3
At equilibrium?
yes
&
83
K=
At equilibrium?
no
Oyes
32
no
G
K=
9
K=4
Explanation
Check
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80
*
B
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52
F3
FS
A
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F28
F12
Predict the product of this organic reaction:
OH
[0]
P+
+ H₂O
Specifically, in the drawing area below draw the skeletal ("line") structure of P.
If there isn't any P because this reaction won't happen, check the No reaction box under the drawing area.
Note for advanced students: you can assume the reaction is run under mild conditions.
Explanation
Check
Click and drag to start drawing a
structure.
ப
G
P
x
©2025 McGraw Hill LLC. All Rights Reserved. Term
Explanation
Check
Draw the condensed structure of a secondary alcohol with 6 carbon atoms, 1 oxygen atom, and no double or triple bonds.
Click anywhere to draw the first
atom of your structure.
G
2025 McGraw Hill LLC. All Rights Reserved. Term
Ć
X
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Chapter 12 Solutions
Organic Chemistry - Standalone book
Ch. 12.2 - Write structural formulas for toluene (C6H5CH3)...Ch. 12.3 - Prob. 2PCh. 12.5 - Prob. 3PCh. 12.5 - Prob. 4PCh. 12.6 - Prob. 5PCh. 12.6 - Chrysene is an aromatic hydrocarbon found in coal...Ch. 12.8 - Prob. 7PCh. 12.9 - As measured by their first-order rate constants,...Ch. 12.9 - Give the structure of the principal organic...Ch. 12.9 - Prob. 10P
Ch. 12.10 - Prob. 11PCh. 12.11 - Prob. 12PCh. 12.12 - Prob. 13PCh. 12.13 - Prob. 14PCh. 12.13 - Prob. 15PCh. 12.15 - The regioselectivity of Birch reduction of...Ch. 12.16 - Prob. 17PCh. 12.17 - Both cyclooctatetraene and styrene have the...Ch. 12.17 - Prob. 19PCh. 12.18 - Give an explanation for each of the following...Ch. 12.19 - Prob. 21PCh. 12.19 - What does a comparison of the heats of combustion...Ch. 12.20 - Prob. 23PCh. 12.20 - Prob. 24PCh. 12.20 - Prob. 25PCh. 12.20 - Prob. 26PCh. 12.20 - Prob. 27PCh. 12.20 - Prob. 28PCh. 12.21 - Prob. 29PCh. 12.21 - Prob. 30PCh. 12.22 - Prob. 31PCh. 12.22 - Prob. 32PCh. 12 - Write structural formulas and give the IUPAC names...Ch. 12 - Prob. 34PCh. 12 - Prob. 35PCh. 12 - Prob. 36PCh. 12 - Prob. 37PCh. 12 - Acridine is a heterocyclic aromatic compound...Ch. 12 - Prob. 39PCh. 12 - Prob. 40PCh. 12 - Prob. 41PCh. 12 - Evaluate each of the following processes applied...Ch. 12 - Prob. 43PCh. 12 - Prob. 44PCh. 12 - Prob. 45PCh. 12 - Prob. 46PCh. 12 - Anthracene undergoes a DielsAlder reaction with...Ch. 12 - Prob. 48PCh. 12 - Prob. 49PCh. 12 - The relative rates of reaction of ethane, toluene,...Ch. 12 - Both 1,2-dihydronaphthalene and...Ch. 12 - Prob. 52PCh. 12 - Prob. 53PCh. 12 - Prob. 54PCh. 12 - Prob. 55PCh. 12 - Prob. 56PCh. 12 - Each of the following reactions has been described...Ch. 12 - Prob. 58PCh. 12 - A compound was obtained from a natural product and...Ch. 12 - Prob. 60PCh. 12 - Suggest reagents suitable for carrying out each of...Ch. 12 - Prob. 62PCh. 12 - Prob. 63DSPCh. 12 - Prob. 64DSPCh. 12 - Prob. 65DSPCh. 12 - Prob. 66DSP
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- Highlight in red the primary carbons in this molecule. Highlight the quaternary carbons in blue. OH Garrow_forwardDraw the condensed structure of a secondary alcohol with 6 carbon atoms, 1 oxygen atom, and no double or triple bonds. Click anywhere to draw the first atom of your structure. Explanation Check ם' G P x 2025 McGraw Hill LLC. All Rights Reserved. Terms of Usarrow_forwardWhat is the missing reactant in this organic reaction? [0] H R + H2O Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there is no reasonable possibility for R, check the No answer box under the drawing area. Click and drag to start drawing a structure. :arrow_forward
- Indicate the correct answer:(A) Paper and diamond are polymeric materials.(B) Fiberglass and Teflon are polymeric materials.(C) Teflon and paper are composite materials.(D) Diamond and fiberglass are ceramic materials.arrow_forwardDraw the major product formed in the reaction. Be sure to draw a hydrogen on any heteroatoms, where applicable. NaCN ethanol water Select Draw Templates More Erasearrow_forwardPredict the major products of the following organic reaction: Some important Notes: Draw the major product, or products, of the reaction in the drawing area below. If there aren't any products, because no reaction will take place, check the box below the drawing area instead. Be sure to draw bonds carefully to show important geometric relationships between substituents. Note: if your answer contains a complicated ring structure, you must use one of the molecular fragment stamps (available in the menu at right) to enter the ring structure. You can add any substituents using the pencil tool in the usual way.arrow_forward
- Indicate the correct answer:(A) Paper and diamond are polymeric materials.(B) Fiberglass and Teflon are polymeric materials.(C) Teflon and paper are composite materials.(D) Diamond and fiberglass are ceramic materials.arrow_forwardve two substances in each sample can interconvert. That is, each kind of molecule can turn into the other. The equilibrium constant K for each interconversion equilibrium is shown below the sketch. Decide whether each solution is at equilibrium. 1 க K= 4 At equilibrium? K= At equilibrium? Oyes O no yes no cib 818 814 K=1 K=2 Explanation Check G 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardDraw the major product for each of the reactions, showing the correct stereochemistry, if any. Draw hydrogen atoms on chirality centers.arrow_forward
- A thermosetting polymer(A). When heated again, it can be remolded or softened.(B). It has great elasticity, so it can stretch to several times its initial length and return to its original size.(C). It is formed by hydrogen bonds.(D). It has a rigid behavior due to its cross-linked bonds.arrow_forwardComplete the electron-pushing mechanism for the given ether synthesis from propanol in concentrated sulfuric acid at 140°C by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Draw hydrogens bonded to oxygen, where applicable.arrow_forwardDetermine whether the following reaction is an example of a nucleophilic substitution reaction: Br HO. OH + X Br + Molecule A Molecule B Is this a nucleophilic substitution reaction? Explanation Check G Yes No P d+ 2025 McGraw Hill LLC. All Rights Reserved. Term Xarrow_forward
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