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ORGANIC CHEMISTRY-WILEYPLUS NEXTGEN
4th Edition
ISBN: 9781119760924
Author: Klein
Publisher: WILEY
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Chapter 2, Problem 67ASP
Interpretation Introduction
Interpretation: The bond-line drawing of
Concept Introduction: A method used to represent molecular structures of compounds is said to be bond line notation. In this notation, a line depicts a bond between two atoms and are drawn in a zigzag format.
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Students have asked these similar questions
Which of the following carbon to carbon bonds has the shortest bond?
H.
H.
H.
C=C
- C-H
-
H.
H
H.
H.
Option 1
Option 2
Option 3
either A or B
Which resonance structure below holds the negative charge better.
A
B
C
H3C
H₂C
H₂C
Select one:
a. A
b. B
C. C
CH3
CH 3
CH 3
Exothermic
1. Fill in the following table for endothermic and exothermic reactions:
Endothermic n no so
Absorb or release heat
Positive or negative AH
Products or reactants have higher energy
Products or reactant more stable
Favorable or unfavorable
Bonds stronger in reactants or products
2. Circle the compound in each pair that has the higher bond dissociation energy/stronger bond:
a.
NH3 or PH3
b. H2Se or H2S
с.
CH4 or SIH4
Use AH and the balanced equation below to answer question 3
C,H12O6→ 2 C;H,O + 2 CO2 AH = -16.0 kcal
3. How many kcal would be released from:
a. 6.00 mols of C,H12O6 reacting
b. 2.13 mols of C¿HO being produced
c. 20.0g grams C,H12O6 (180.1559 g/mol) reacting
4. Considering the reaction: O3 + NO → 02 + NO2, circle the impact on reaction rate of the following:
a. Increasing concentration of O3: increase / decrease rate
b. Decreased concentration of NO: increase / decrease rate
c. Increased temperature: increase / decrease rate
Chapter 2 Solutions
ORGANIC CHEMISTRY-WILEYPLUS NEXTGEN
Ch. 2.1 - Prob. 1LTSCh. 2.1 - Prob. 3ATSCh. 2.2 - Prob. 2LTSCh. 2.2 - Prob. 4PTSCh. 2.2 - Prob. 6ATSCh. 2.4 - Prob. 3LTSCh. 2.4 - Prob. 9ATSCh. 2.5 - Prob. 4LTSCh. 2.5 - Prob. 11PTSCh. 2.9 - Prob. 6LTS
Ch. 2.9 - Prob. 15PTSCh. 2.9 - Prob. 16PTSCh. 2.10 - Prob. 18CCCh. 2.10 - Prob. 19CCCh. 2.10 - Prob. 20CCCh. 2.10 - Prob. 21CCCh. 2.10 - Prob. 22CCCh. 2.10 - Prob. 23CCCh. 2.10 - Prob. 24CCCh. 2.10 - Prob. 25CCCh. 2 - Prob. 34PPCh. 2 - Prob. 35PPCh. 2 - Prob. 36PPCh. 2 - Prob. 37PPCh. 2 - Prob. 38PPCh. 2 - Prob. 40PPCh. 2 - Prob. 42PPCh. 2 - Prob. 43PPCh. 2 - Prob. 44PPCh. 2 - Prob. 45PPCh. 2 - Prob. 46PPCh. 2 - Prob. 47PPCh. 2 - Prob. 48PPCh. 2 - Prob. 49PPCh. 2 - Prob. 50PPCh. 2 - Prob. 67ASP
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- 4. Identify which of the structures below correspond to a. b. C. d. CH,CH,CH,CH(CH3)2 f. (CH3)2(CH2)2CH(CH3)2 (CH3)2CH₂CH₂CH(CH3)2 CH3(CH2)2CH(CH3)2 e. g. h. H H H H—C—C—C—C | H H H с H H H I C-H CIHarrow_forwardH₂C a. How many polar bond(s) is (are) present in this molecule? b. What is the most electronegative atom present in this molecule? c. What is the least electronegative atom present in this molecule? N * For the C-0 bond, what is the direction of the dipole moment (from 3+ to 2-)? Use either 'up' or 'down' for your answer inaný 0=6 $ -0 to de % CH3 A hparrow_forwardWhat is the correct Lewis structure for acetaldehyde, an aldehyde which has the molecular formula CH,O? H :0 :0 H- H :0: H :0: H -č: FC-H H- -H H- -C-H H- C -ċ-H H- H H H a b d e a. Ob. Oc. Od. Oe.arrow_forward
- Stalevo is the trade name for a medication used for Parkinson's disease, which contains L-dopa, carbidopa, and entacapone. a. Draw a Lewis structure for entacapone. b. Which C–C bond in entacapone is the longest? c. Which C–C single bond is the shortest? d. Which C–N bond is the longest? e Which C–N bond is the shortest? f. Use curved arrows to draw a resonance structure that is an equal contributor to the resonance hybrid. g. Use curved arrows to draw a resonance structure that is a minor contributor to the resonance hybrid.arrow_forwardConsider a molecule of methanimine (CH3N) compared to a molecule of methylamine (CH5N). The C-N bond in methanimine is than the C-N bond in methylamine. A. longer and stronger B. longer and weaker C. shorter and stronger D. shorter and weaker E. the same strength and length asarrow_forward3. Resonance forms of the acetate ion are below. :0: :0: :0: H3C H3C H3C А C a. Provide arrows that show electron movement from A to B and B to C. b. Two of these resonance forms are identical. Which two are actually the same? C. Which is the "least contributing" resonance form (A, B, or C)? Briefly explain your choice. d. Draw the resonance hybrid for the acetate ion (use "delta" &+ or- to show partial charges).arrow_forward
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