EBK ORGANIC CHEMISTRY-PRINT COMPANION (
4th Edition
ISBN: 9781119776741
Author: Klein
Publisher: WILEY CONS
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 7.7, Problem 14ATS
Interpretation Introduction
Interpretation:
The major product for the given elimination reaction must be drawn. The reason for the formation of only one product must also be explained.
Concept introduction:
If a strong base is used during elimination, it is less selective and in most cases, hydrogen is abstracted from less sterically crowded carbon. Generally, the two anti-periplanar groups are eliminated and
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Pyrethrins, such as jasmolin II (shown below), are a group of natural compounds that are synthesized
by flowers of the genus Chrysanthemum (known as pyrethrum flowers) to act as insecticides.
CH3
CH2=CH-CH.
CH-C-
-HCS
0-CH,
CH,-C
H2C-
ČH,
Which is not a functional group or structural feature in jasmolin II?
cycloalkane
carboxylic acid
ester
alkene
21.) Calculate the enthalpy of hydrogenation of benzene to cyclohexane from the following
reactions
A,H (kJ/mol)
C6H6 (1) + 15/2 02 (g) → 6 CO2 (g) + 3 H20 (1)
C6H12 (1) + 9 02 (g) → 6 CO2 (g) + 6 H20 (1)
H2 (g) + ½ 02 (g) → H2O (1)
-3268
-3920
-285.83
a.) -205 kJ/mol
b.) -1507 kJ/mol
c.) -938 kJ/mol
d.) -366 kJ/mol
Write the systematic name of each organic molecule:
structure
O
||
H-C—CH-CH3
OH
H—C–CH2–CH2–CH3
||
HỌ—CH,—CH,—CH–CH
OH
name
Ú
0
0
Chapter 7 Solutions
EBK ORGANIC CHEMISTRY-PRINT COMPANION (
Ch. 7.2 - Prob. 1CCCh. 7.3 - Prob. 2CCCh. 7.3 - Prob. 1LTSCh. 7.3 - Prob. 3PTSCh. 7.3 - Prob. 4ATSCh. 7.3 - Prob. 2LTSCh. 7.3 - Prob. 5PTSCh. 7.3 - Prob. 6ATSCh. 7.3 - Prob. 7CCCh. 7.4 - Prob. 8CC
Ch. 7.5 - Prob. 9CCCh. 7.6 - Prob. 10CCCh. 7.6 - Prob. 11CCCh. 7.7 - Prob. 12PTSCh. 7.7 - Prob. 13PTSCh. 7.7 - Prob. 14ATSCh. 7.7 - Prob. 4LTSCh. 7.7 - Prob. 16ATSCh. 7.7 - Prob. 17CCCh. 7.7 - Prob. 18CCCh. 7.7 - Prob. 5LTSCh. 7.7 - Prob. 19PTSCh. 7.7 - Prob. 20ATSCh. 7.8 - Prob. 21PTSCh. 7.8 - Prob. 22ATSCh. 7.8 - Prob. 23CCCh. 7.8 - Prob. 24CCCh. 7.8 - Prob. 25CCCh. 7.8 - Prob. 26CCCh. 7.8 - Prob. 27CCCh. 7.9 - Prob. 7LTSCh. 7.9 - Prob. 29ATSCh. 7.9 - Prob. 30ATSCh. 7.9 - Prob. 31ATSCh. 7.10 - Prob. 32CCCh. 7.10 - Prob. 33CCCh. 7.10 - Prob. 34CCCh. 7.11 - Prob. 8LTSCh. 7.11 - Prob. 35PTSCh. 7.11 - Prob. 36PTSCh. 7.11 - Prob. 37ATSCh. 7.11 - Prob. 9LTSCh. 7.11 - Prob. 40PTSCh. 7.11 - Prob. 41ATSCh. 7.12 - Prob. 42CCCh. 7.12 - Prob. 43CCCh. 7.12 - Prob. 44CCCh. 7.12 - Prob. 45CCCh. 7.12 - Prob. 46CCCh. 7 - Prob. 47PPCh. 7 - Prob. 48PPCh. 7 - Prob. 49PPCh. 7 - Prob. 50PPCh. 7 - Prob. 51PPCh. 7 - Prob. 52PPCh. 7 - Prob. 53PPCh. 7 - Prob. 54PPCh. 7 - Prob. 55PPCh. 7 - Prob. 56PPCh. 7 - Prob. 57PPCh. 7 - Prob. 58PPCh. 7 - Prob. 59PPCh. 7 - Prob. 60PPCh. 7 - Prob. 61PPCh. 7 - Prob. 64PPCh. 7 - Indicate whether you would use NaOEt or tBuOK to...Ch. 7 - Prob. 68PPCh. 7 - Draw a plausible mechanism for each of the...Ch. 7 - Prob. 70PPCh. 7 - Prob. 71PPCh. 7 - Prob. 72PPCh. 7 - Prob. 73PPCh. 7 - Prob. 74PPCh. 7 - Prob. 77PPCh. 7 - Prob. 78PPCh. 7 - Prob. 81ASPCh. 7 - Prob. 87ASPCh. 7 - Prob. 90ASPCh. 7 - Prob. 91IPCh. 7 - Prob. 92IPCh. 7 - Prob. 93IPCh. 7 - Prob. 94IPCh. 7 - Prob. 95IPCh. 7 - Prob. 96IPCh. 7 - Prob. 97IPCh. 7 - Prob. 98IPCh. 7 - Prob. 99IPCh. 7 - Prob. 100IPCh. 7 - Prob. 101IPCh. 7 - Prob. 102IPCh. 7 - Prob. 103IPCh. 7 - Prob. 105IPCh. 7 - Prob. 106IPCh. 7 - Prob. 107IPCh. 7 - Prob. 109IPCh. 7 - Prob. 110CPCh. 7 - Prob. 112CPCh. 7 - Prob. 114CP
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
- Formaldehyde, H2C=O, is known to all biologists because of its usefulness as a tissue preservative. When pure, formaldehyde trimerizes to give trioxane, C3H6O3, which, surprisingly enough, has no carbonyl groups. Only one monobromo derivative (C3H5BrO3) of trioxane is possible. Propose a structure for trioxane.arrow_forwardDodecane, C12H26, is an unbranched alkane Predict the following: Will it dissolve in water? Will it dissolve in hexane? Will it burn when ignited? Is it a liquid, solid, or gas at room temperature and atmospheric pressure? Is it more or less dense than water?arrow_forwardWhat structural features help us identify a compound as(a) an alkane, (b) a cycloalkane, (c) an alkene, (d) an alkyne,(e) a saturated hydrocarbon, (f) an aromatic hydrocarbon?arrow_forward
- 12. Write bond-line structural formulas for (a.) two primary alcohols, (b.) a secondary alcohol, and (c.) a tertiary alcohol-all having the molecular formula CaH100.arrow_forwardWhat are the products formed from the following reactions: 1) The addition of dimethylborane (Me2BH) to ethylene 2) The addition of dimethylborane (Me2BH) to acetylene Please include the formulas for the products as well. Thank you!arrow_forward8. Three compounds, G, H and J are structural isomers. They have the molecular formula C3H$O. Their chemical properties are given below: React with 2,4-dinitrophenylhydrazine to form yellow precipitate. G is resistant to oxidation. H is oxidised to L (C7H6O2) J is oxidised to M (C8H6O4) Write the structural formula of G, H, J, L and M. Outline one chemical test to distinguish between G and H.arrow_forward
- A hydrocarbon C5H12 gives only one mono-chlorination product. Identify the hydrocarbon.arrow_forward2,2,3,3-Tetrabromopentane can be prepared by an addition reaction of excess Br2 with an alkyne. Draw the structure of the alkyne and name it.arrow_forwardIn an advanced analytical chemistry lab, a team analyzing a compound 'Q' known to be a structural isomer of octane (C8H18). To determine the specific structure of 'Q', a series of spectroscopic analyses are performed. The sequence of the analysis involves: Infrared (IR) spectroscopy, which indicates the absence of functional groups like alcohols, ketones, and carboxylic acids. Nuclear Magnetic Resonance (NMR) spectroscopy, showing signals indicative of only methyl and methylene groups, with no evidence of methine (CH) or quaternary carbon environments. Mass spectrometry (MS), revealing a fragmentation pattern consistent with branched alkane structures. Based on this sequence of analyses, what is the most likely structure of compound 'Q'? Options: A. 2,2,4- Trimethylpentane B. n-Octane C. 2-Methylheptane D. 3-Ethylhexane Don't use chatgpt please provide valuable answerarrow_forward
- 4d. polysubstituted benzene HO- O2N NO2 NH2 NO2arrow_forwardAn alkene having 7 carbon atoms has Molecular formula and its name is O C;H14, heptene O C7H14, hexene C7H16, heptane O GH12, heptynearrow_forwardA student added bromine solution to a hydrocarbon sample that contained an isomer of C6H12 (E) in the absence of light. After shaking the sample, the student noticed that the colour of the bromine solution changed from orange to colourless. Use the following information to answer the question 6. An interpretation that could be made from the student's observations is that the hydrocarbon sample isi and the IUPAC name of the sample could be ii . The statement above is completed by the information in row: i saturated saturated unsaturated unsaturated Row A B C D wer (2 marks) ii hex-2-ene cyclopentane hex-2-ene cyclopentane 0arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License