ORGANIC CHEMISTRY-PRINT (LL)-W/WILEY
4th Edition
ISBN: 9781119761105
Author: Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 1.12, Problem 29ATS
Interpretation Introduction
Interpretation: Whether diphenyl ether exhibits molecular dipole moment or not should be identified and if it does then the direction of the net molecular dipole moment must be indicated.
Concept Introduction: The arrangement of electron pairs is identified according to VSEPR (Valence Shell Electron Pair Repulsion) theory wherein all the electron pairs are aligned in such a way that they are at maximum distance from each other. The structure of every molecule in VSEPR is explained by considering the steric number (combination of lone pairs and
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Please help answer
Q3- Rank the following molecule according to their increasing stability. Where 1 is the least stable and 4
is the most stable.
CH3
C(CH3)3
CH(CH3)2
Q4- Rank the following molecule according to their increasing dipole moment. Where 1 is the lowest
dipole moment and 4 is the largest dipole moment.
CI
Br
F
Account for the fact that among the chlorinated derivatives of methane, chloro-
methane has the largest dipole moment and tetrachloromethane has the smallest
dipole moment.
Molecular
Formula
Dipole Moment
(debyes, D)
Name
CH,CI
CH,CI,
Chloromethane
1.87
Dichloromethane
1.60
Trichloromethane
CHCI,
1.01
Tetrachloromethane
CCI,
Chapter 1 Solutions
ORGANIC CHEMISTRY-PRINT (LL)-W/WILEY
Ch. 1.2 - Prob. 1LTSCh. 1.2 - Prob. 2ATSCh. 1.2 - Prob. 2LTSCh. 1.3 - Prob. 3LTSCh. 1.3 - Prob. 4PTSCh. 1.3 - Prob. 5PTSCh. 1.4 - Prob. 4LTSCh. 1.4 - Prob. 7PTSCh. 1.4 - Prob. 8PTSCh. 1.4 - Prob. 9ATS
Ch. 1.5 - Prob. 5LTSCh. 1.5 - Prob. 10PTSCh. 1.5 - Prob. 11ATSCh. 1.5 - Prob. 12ATSCh. 1.6 - Prob. 6LTSCh. 1.6 - Prob. 14ATSCh. 1.7 - Prob. 7LTSCh. 1.7 - Prob. 17ATSCh. 1.10 - Prob. 18CCCh. 1.10 - Prob. 20CCCh. 1.10 - Prob. 8LTSCh. 1.10 - Prob. 21PTSCh. 1.10 - Nemotin is a compound that was first isolated from...Ch. 1.10 - Prob. 23CCCh. 1.11 - Prob. 9LTSCh. 1.11 - Prob. 24PTSCh. 1.11 - Prob. 25PTSCh. 1.11 - Prob. 26PTSCh. 1.11 - Prob. 27ATSCh. 1.12 - Prob. 10LTSCh. 1.12 - Prob. 29ATSCh. 1.13 - Prob. 11LTSCh. 1.13 - Prob. 31ATSCh. 1 - Prob. 32PPCh. 1 - Prob. 33PPCh. 1 - Prob. 34PPCh. 1 - Prob. 35PPCh. 1 - Prob. 36PPCh. 1 - Prob. 37PPCh. 1 - Prob. 38PPCh. 1 - Prob. 39PPCh. 1 - Prob. 40PPCh. 1 - Prob. 41PPCh. 1 - Prob. 42PPCh. 1 - Prob. 44PPCh. 1 - Prob. 45PPCh. 1 - Prob. 46PPCh. 1 - Prob. 47PPCh. 1 - Prob. 48PPCh. 1 - Prob. 49PPCh. 1 - Prob. 50PPCh. 1 - Prob. 51PPCh. 1 - Prob. 52PPCh. 1 - Prob. 53PPCh. 1 - Prob. 54PPCh. 1 - Nicotine is an addictive substance found in...Ch. 1 - Prob. 56PPCh. 1 - Prob. 57PPCh. 1 - Prob. 59PPCh. 1 - Prob. 63ASPCh. 1 - Prob. 64ASPCh. 1 - Prob. 66ASPCh. 1 - Prob. 69ASPCh. 1 - Prob. 71ASPCh. 1 - Prob. 72ASPCh. 1 - Prob. 75IP
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
- Consider a solvatochromic compound that is blue in water and orange in acetone. Which of the following statements about this compound is true? Group of answer choices The compound exhibits positive solvatochromism The compound exhibits negative solvatochromism In ethanol - a solvent with a polarity between those of water and acetone - the compound would be yellow in color The HOMO is more stabilized by polar solvents than the LUMOarrow_forwardcompound HO at 6 and NO2 at 1arrow_forward6. The mendelic acid "chemical face peel" is a relatively new innovation for the rejuvenation of problem skin. In addition to removing dead skin cells, its antibacterial properties help acne-prone skin. The technique has also been touted as a way to improve hyperpigmentation due to post acne scarring. Although the compound was first derived from bitter almonds, mendelic acid is generally now synthesized in the laboratory. To formulate one of these "face peel" emulsions, you are asked to prepare as much pH = 3.543 buffer solution as you can from 100.00 mL of 0.5000 M mendelic acid (HMend). Since the use of mendelic acid is relatively new, the conjugate base mendolate (Mend) cannot be purchased. Fortunately, you have plenty of 0.4018 M NaOH. Ka = 3.894x 10-4 for mendelic acid. How would you prepare the buffer solution? The following questions will guide you to find the final answer. A B. C. What is the moles ratio between the equilibrium molarity of mendelic acid (MA) and mendolate?…arrow_forward
- 6. The mendelic acid "chemical face peel" is a relatively new innovation for the rejuvenation of problem skin. In addition to removing dead skin cells, its antibacterial properties help acne-prone skin. The technique has also been touted as a way to improve hyperpigmentation due to post acne scarring. Although the compound was first derived from bitter almonds, mendelic acid is generally now synthesized in the laboratory. To formulate one of these "face peel" emulsions, you are asked to prepare as much pH = 3.799 buffer solution as you can from 100.00 mL of 0.5000 M mendelic acid (HMend). Since the use of mendelic acid is relatively new, the conjugate base mendolate (Mend) cannot be purchased. Fortunately, you have plenty of 0.4087 M NaOH. Ka = 3.894x10-4 for mendelic acid. How would you prepare the buffer solution? The following questions will guide you to find the final answer. What is the moles ratio between the equilibrium molarity of mendelic acid (MA) and mendolate? Please…arrow_forwardDraw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the carboxy with the para position in benzoic acid.arrow_forwardWhat are the dipole moments of cathechol resorcinol and hydroquinol ? Give their possible directionsarrow_forward
- Pleasearrow_forward1. The structure of pyridine and pyrrole is given below along with the dipole moment of each molecule. Explain why the nitrogen is the negative end of the dipole in pyridine, while in pyrrole it is the positive end of the dipole. Use structures to support your argument. Pyridine Pyrrolearrow_forwarddipole moment of phenol is smaller than that of methanol. Why?arrow_forward
- 16-17 Propylamine (bp 48°C), ethylmethylamine (bp 37°C), and trimethylamine (bp 3°C) are constitutional isomers with the molecular formula C3HgN. Account for the fact that trimethylamine has the lowest boiling point of the three and propylamine has the highest.arrow_forwardSpecify whether you expect a molecular dipole moment for each of the following compounds. ball & stick ✓ H3C + labels CH3 Dipole : ball & stick ✓ + labels H2₂C=CCI2 Dipole :arrow_forward6) Tell what kinds of orbitals on each atom overlap to form the carbon-carbon and carbon-hydrogen bonds.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Principles of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher: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: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Principles of Modern Chemistry
Chemistry
ISBN:9781305079113
Author:David W. Oxtoby, H. Pat Gillis, Laurie J. Butler
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
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Mass Spectrometry; Author: Professor Dave Explains;https://www.youtube.com/watch?v=hSirWciIvSg;License: Standard YouTube License, CC-BY