GENERAL CHEMISTRY ACHIEVE ACCESS W/BOOK
4th Edition
ISBN: 9781319405212
Author: McQuarrie
Publisher: MAC HIGHER
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 8, Problem 8.45P
Interpretation Introduction
Interpretation:
The possible geometric isomers of dichloroethane have to be given.
Concept Introduction:
Isomers:
The molecules, which have the same molecular formula but different arrangement of atom, are called as isomers. There are two types of isomers,
- Structural isomers
- Stereo isomers
Stereo isomers:
Stereo isomers are the isomers that have same molecular formula but differ in spatial arrangement of atoms. Stereo isomers can be sub divided into two groups,
- Optical isomers
- Geometric isomers
Optical isomers:
Optical isomers are the mirror image of a molecule and they can be rotated by plane polarized light.
Geometric isomers:
If there is restricted rotation in a molecule there arises geometric isomerism. Geometric isomers are also known as cis- Trans isomerism.
- If the two atoms locked in same side of the molecule then it is called as cis isomers.
- If the two atoms locked in opposite side of the molecule then it is called as trans isomers.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Draw the product of the reaction shown below. Ignore small byproducts that would evaporate please.
Relative Abundance
20-
Problems
501
(b) The infrared spectrum has a medium-intensity peak at about 1650 cm. There is also a
C-H out-of-plane bending peak near 880 cm.
100-
80-
56
41
69
M(84)
LL
15 20 25
30
35
55 60 65 70
75
80
85 90
m/z
Polyethylene furanoate is a polymer made from plant-based sources; it is used for packaging. Identify the monomer(s) used in the production of this polymer using a condensation process.
Chapter 8 Solutions
GENERAL CHEMISTRY ACHIEVE ACCESS W/BOOK
Ch. 8 - Prob. 8.1PCh. 8 - Prob. 8.2PCh. 8 - Prob. 8.3PCh. 8 - Prob. 8.4PCh. 8 - Prob. 8.5PCh. 8 - Prob. 8.6PCh. 8 - Prob. 8.7PCh. 8 - Prob. 8.8PCh. 8 - Prob. 8.9PCh. 8 - Prob. 8.10P
Ch. 8 - Prob. 8.11PCh. 8 - Prob. 8.12PCh. 8 - Prob. 8.13PCh. 8 - Prob. 8.14PCh. 8 - Prob. 8.15PCh. 8 - Prob. 8.16PCh. 8 - Prob. 8.17PCh. 8 - Prob. 8.18PCh. 8 - Prob. 8.19PCh. 8 - Prob. 8.20PCh. 8 - Prob. 8.21PCh. 8 - Prob. 8.22PCh. 8 - Prob. 8.23PCh. 8 - Prob. 8.24PCh. 8 - Prob. 8.25PCh. 8 - Prob. 8.26PCh. 8 - Prob. 8.27PCh. 8 - Prob. 8.28PCh. 8 - Prob. 8.29PCh. 8 - Prob. 8.30PCh. 8 - Prob. 8.31PCh. 8 - Prob. 8.32PCh. 8 - Prob. 8.33PCh. 8 - Prob. 8.34PCh. 8 - Prob. 8.35PCh. 8 - Prob. 8.36PCh. 8 - Prob. 8.37PCh. 8 - Prob. 8.38PCh. 8 - Prob. 8.39PCh. 8 - Prob. 8.40PCh. 8 - Prob. 8.41PCh. 8 - Prob. 8.42PCh. 8 - Prob. 8.43PCh. 8 - Prob. 8.44PCh. 8 - Prob. 8.45PCh. 8 - Prob. 8.46PCh. 8 - Prob. 8.47PCh. 8 - Prob. 8.48PCh. 8 - Prob. 8.49PCh. 8 - Prob. 8.50PCh. 8 - Prob. 8.51PCh. 8 - Prob. 8.52PCh. 8 - Prob. 8.53PCh. 8 - Prob. 8.54PCh. 8 - Prob. 8.55PCh. 8 - Prob. 8.56PCh. 8 - Prob. 8.57PCh. 8 - Prob. 8.59PCh. 8 - Prob. 8.60PCh. 8 - Prob. 8.61PCh. 8 - Prob. 8.62PCh. 8 - Prob. 8.63PCh. 8 - Prob. 8.64PCh. 8 - Prob. 8.65PCh. 8 - Prob. 8.66PCh. 8 - Prob. 8.67PCh. 8 - Prob. 8.69PCh. 8 - Prob. 8.70PCh. 8 - Prob. 8.71PCh. 8 - Prob. 8.72PCh. 8 - Prob. 8.73PCh. 8 - Prob. 8.74PCh. 8 - Prob. 8.75PCh. 8 - Prob. 8.76PCh. 8 - Prob. 8.77PCh. 8 - Prob. 8.78PCh. 8 - Prob. 8.79PCh. 8 - Prob. 8.80P
Knowledge Booster
Learn more about
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
- Phenol is the starting material for the synthesis of 2,3,4,5,6-pentachlorophenol, known al-ternatively as pentachlorophenol, or more simply as penta. At one time, penta was widely used as a wood preservative for decks, siding, and outdoor wood furniture. Draw the structural formula for pentachlorophenol and describe its synthesis from phenol.arrow_forward12 Mass Spectrometry (d) This unknown contains oxygen, but it does not show any significant infrared absorption peaks above 3000 cm . 59 100- BO 40 Relative Abundance M(102) - 15 20 25 30 35 40 45 50 5 60 65 70 75 80 85 90 95 100 105 mizarrow_forwardDraw a Haworth projection of a common cyclic form of this monosaccharide: H HO H HO H HO H H -OH CH2OH Click and drag to start drawing a structure. Х : Darrow_forward
- : Draw the structure of valylasparagine, a dipeptide made from valine and asparagine, as it would appear at physiological pH. Click and drag to start drawing a structure. P Darrow_forwardDraw the Haworth projection of α-L-mannose. You will find helpful information in the ALEKS Data resource. Click and drag to start drawing a structure. : ཊི Х Darrow_forwardDraw the structure of serine at pH 6.8. Click and drag to start drawing a structure. : d كarrow_forward
- Take a look at this molecule, and then answer the questions in the table below it. CH2OH H H H OH OH OH CH2OH H H H H OH H H OH H OH Is this a reducing sugar? yes α β ロ→ロ no ☑ yes Does this molecule contain a glycosidic bond? If you said this molecule does contain a glycosidic bond, write the symbol describing it. O no 0+0 If you said this molecule does contain a glycosidic bond, write the common names (including anomer and enantiomer labels) of the molecules that would be released if that bond were hydrolyzed. If there's more than one molecule, separate each name with a comma. ☐arrow_forwardAnswer the questions in the table below about this molecule: H₂N-CH₂ -C—NH–CH–C—NH–CH—COO- CH3 CH CH3 What kind of molecule is this? 0= CH2 C If you said the molecule is a peptide, write a description of it using 3-letter codes separated ☐ by dashes. polysaccharide peptide amino acid phospolipid none of the above Хarrow_forwardDraw a Haworth projection of a common cyclic form of this monosaccharide: CH₂OH C=O HO H H -OH H OH CH₂OH Click and drag to start drawing a structure. : ☐ Х S '☐arrow_forward
- Nucleophilic Aromatic Substitution 22.30 Predict all possible products formed from the following nucleophilic substitution reactions. (a) (b) 9 1. NaOH 2. HCI, H₂O CI NH₁(!) +NaNH, -33°C 1. NaOH 2. HCl, H₂Oarrow_forwardSyntheses 22.35 Show how to convert toluene to these compounds. (a) -CH,Br (b) Br- -CH3 22.36 Show how to prepare each compound from 1-phenyl-1-propanone. 1-Phenyl-1-propanone ہتی. Br. (b) Br (racemic) 22.37 Show how to convert ethyl benzene to (a) 2,5-dichlorobenzoic acid and (b) 2,4-dichlorobenzoic acid. 22.38 Show reagents and conditions to bring about the following conversions. (a) 9 NH2 8 CO₂H NH2 CO₂Et (d) NO2 NH2 S NH₂ NO2 CHS CHarrow_forwardive the major organic product(s) of each of the following reactions or sequences of reactions. Show all rant stereochemistry. [10 only] A. B. NaN3 1. LiAlH4, ether Br 2. H₂O CH3 HNO3 H₂/Pt H₂SO ethanol C. 0 0 CH3CC1 NaOH NHCCH AICI H₂O . NH₂ CH3CH2 N CH2CH3 + HCI CH₂CH 3 1. LIAIH, THE 2. H₂Oarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY