Chemistry: An Introduction to General, Organic, and Biological Chemistry Plus Mastering Chemistry with Pearson eText -- Access Card Package (13th Edition)
13th Edition
ISBN: 9780134416793
Author: Karen C Timberlake
Publisher: PEARSON
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Textbook Question
Chapter 11, Problem 11.60APP
Draw the line-angle formula for each of the following: (11.8)
a. 3-chlorophenol
b. 1,4-dichlorobenzene
c. 2-bromotoluene
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3. Consider the compounds below and determine if they are aromatic, antiaromatic, or
non-aromatic. In case of aromatic or anti-aromatic, please indicate number of I
electrons in the respective systems. (Hint: 1. Not all lone pair electrons were explicitly
drawn and you should be able to tell that the bonding electrons and lone pair electrons
should reside in which hybridized atomic orbital 2. You should consider ring strain-
flexibility and steric repulsion that facilitates adoption of aromaticity or avoidance of anti-
aromaticity)
H H
N
N:
NH2
N
Aromaticity
(Circle)
Aromatic Aromatic Aromatic Aromatic Aromatic
Antiaromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic
nonaromatic nonaromatic nonaromatic nonaromatic nonaromatic
aromatic TT
electrons
Me
H
Me
Aromaticity
(Circle)
Aromatic Aromatic Aromatic
Aromatic Aromatic
Antiaromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic
nonaromatic nonaromatic nonaromatic nonaromatic nonaromatic
aromatic πT
electrons
H
HH…
A chemistry graduate student is studying the rate of this reaction:
2 HI (g) →H2(g) +12(g)
She fills a reaction vessel with HI and measures its concentration as the reaction proceeds:
time
(minutes)
[IH]
0
0.800M
1.0
0.301 M
2.0
0.185 M
3.0
0.134M
4.0
0.105 M
Use this data to answer the following questions.
Write the rate law for this reaction.
rate
= 0
Calculate the value of the rate constant k.
k =
Round your answer to 2 significant digits. Also be
sure your answer has the correct unit symbol.
None
Chapter 11 Solutions
Chemistry: An Introduction to General, Organic, and Biological Chemistry Plus Mastering Chemistry with Pearson eText -- Access Card Package (13th Edition)
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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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- in which spectral range of EMR, atomic and ionic lines of metal liesarrow_forwardQ2: Label the following molecules as chiral or achiral, and label each stereocenter as R or S. CI CH3 CH3 NH2 C CH3 CH3 Br CH3 X &p Bra 'CH 3 "CH3 X Br CH3 Me - N OMe O DuckDuckarrow_forward1. For the four structures provided, Please answer the following questions in the table below. a. Please draw π molecular orbital diagram (use the polygon-and-circle method if appropriate) and fill electrons in each molecular orbital b. Please indicate the number of π electrons c. Please indicate if each molecule provided is anti-aromatic, aromatic, or non- aromatic TT MO diagram Number of π e- Aromaticity Evaluation (X choose one) Non-aromatic Aromatic Anti-aromatic || ||| + IVarrow_forward
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