Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
Chapter 2.SE, Problem 28AP
Interpretation Introduction

a) CH2FCl

Interpretation:

The most electronegative element in CH2FCl is to be identified.

Concept introduction:

Electronegativity is the intrinsic ability of an atom to attract the shared pair of electrons in a covalent bond. Metals on the left side of the periodic table attract electron weekly and hence have low electronegativity values. Oxygen, nitrogen and halogens on the right side of the periodic table attract electron strongly and have high electronegativity values. Their position in the periodic table determines the relative values of electronegativity of elements. The electronegativity generally decreases from top to bottom and increases from left to right across the periodic table.

To determine:

The most electronegative element in CH2FCl.

Interpretation Introduction

b) FCH2CH2CH2Br

Interpretation:

The most electronegative element in CH2FCl is to be identified.

Concept introduction:

Electronegativity is the intrinsic ability of an atom to attract the shared pair of electrons in a covalent bond. Metals on the left side of the periodic table attract electron weekly and hence have low electronegativity values. Oxygen, nitrogen and halogens on the right side of the periodic table attract electron strongly and have high electronegativity values. Their position in the periodic table determines the relative values of electronegativity of elements. The electronegativity generally decreases from top to bottom and increases from left to right across the periodic table.

To determine:

The most electronegative element in FCH2CH2CH2Br.

Interpretation Introduction

c) HOCH2CH2NH2

Interpretation:

The most electronegative element in CH2FCl is to be identified.

Concept introduction:

Electronegativity is the intrinsic ability of an atom to attract the shared pair of electrons in a covalent bond. Metals on the left side of the periodic table attract electron weekly and hence have low electronegativity values. Oxygen, nitrogen and halogens on the right side of the periodic table attract electron strongly and have high electronegativity values. Their position in the periodic table determines the relative values of electronegativity of elements. The electronegativity generally decreases from top to bottom and increases from left to right across the periodic table.

To determine:

The most electronegative element in HOCH2CH2NH2.

Interpretation Introduction

d) CH3OCH2 Li

Interpretation:

The most electronegative element in CH3OCH2Li is to be identified.

Concept introduction:

Electronegativity is the intrinsic ability of an atom to attract the shared pair of electrons in a covalent bond. Metals on the left side of the periodic table attract electron weekly and hence have low electronegativity values. Oxygen, nitrogen and halogens on the right side of the periodic table attract electron strongly and have high electronegativity values. Their position in the periodic table determines the relative values of electronegativity of elements. The electronegativity generally decreases from top to bottom and increases from left to right across the periodic table.

To determine:

The most electronegative element in CH3OCH2Li.

Blurred answer
05:57
Students have asked these similar questions
compound X has the formula C4H4O3
Explain the structure of the compound using the spectroscopic data. Formula: C9H10O3
What is the nature of the bonding in C3H2F2 , Is it polar?

Chapter 2 Solutions

Organic Chemistry

Ch. 2.7 - Nitric acid (HNO3) reacts with ammonia (NH3) to...Ch. 2.8 - Prob. 12PCh. 2.8 - Amide ion, H2N-, is a much stronger base than...Ch. 2.9 - Prob. 14PCh. 2.9 - Prob. 15PCh. 2.9 - Prob. 16PCh. 2.11 - Using curved arrows, show how the species in part...Ch. 2.11 - Prob. 18PCh. 2.12 - Of the two vitamins A and C, one is hydrophilic...Ch. 2.SE - Prob. 20VCCh. 2.SE - The following model is a representation of...Ch. 2.SE - cis-l, 2-Dichloroethylene and trans-1,...Ch. 2.SE - The following molecular models are representations...Ch. 2.SE - Predict the product(s) of the acid/base reactions...Ch. 2.SE - Use curved arrows to draw the protonated form of...Ch. 2.SE - Prob. 26MPCh. 2.SE - Double bonds can also act like Lewis bases,...Ch. 2.SE - Prob. 28APCh. 2.SE - Use the electronegativity table given in Figure...Ch. 2.SE - Which of the following molecules has a dipole...Ch. 2.SE - Prob. 31APCh. 2.SE - Phosgene, C12C=O, has a smaller dipole moment than...Ch. 2.SE - Prob. 33APCh. 2.SE - Methanethiol, CH3SH, has a substantial dipole...Ch. 2.SE - Calculate the formal charges on the atoms shown in...Ch. 2.SE - Assign formal charges to the atoms in each of the...Ch. 2.SE - Which of the following pairs of structures...Ch. 2.SE - Prob. 38APCh. 2.SE - 1, 3-Cyclobutadiene is a rectangular molecule with...Ch. 2.SE - Alcohols can act either as weak acids or as weak...Ch. 2.SE - The O-H hydrogen in acetic acid is more acidic...Ch. 2.SE - Draw electron-dot structures for the following...Ch. 2.SE - Write the products of the following acid-base...Ch. 2.SE - Rank the following substances in order of...Ch. 2.SE - Which, if any, of the substances in Problem 2-44...Ch. 2.SE - The ammonium ion (NH4+, pKa = 9.25) has a lower...Ch. 2.SE - Prob. 47APCh. 2.SE - Prob. 48APCh. 2.SE - Calculate Ka values from the following pka’s:...Ch. 2.SE - Calculate pKa values from the following Ka’s:...Ch. 2.SE - What is the pH of a 0.050 M solution of formic...Ch. 2.SE - Prob. 52APCh. 2.SE - Maleic acid has a dipole moment, but the closely...Ch. 2.SE - Assume that you have two unlabeled bottles, one of...Ch. 2.SE - Identify the acids and bases in the following...Ch. 2.SE - Which of the following pairs represent resonance...Ch. 2.SE - Draw as many resonance structures as you can for...Ch. 2.SE - Carbocations, which contain a trivalent,...Ch. 2.SE - We’ll see in the next chapter that organic...Ch. 2.SE - The azide functional group, which occurs in...Ch. 2.SE - Phenol, C6H5OH, is a stronger acid than methanol,...Ch. 2.SE - Thiamin diphosphate (TPP), a derivative of vitamin...Ch. 2.SE - Determine if each compound or ion below has a...Ch. 2.SE - Prob. 64APCh. 2.SE - Prob. 65APCh. 2.SE - Draw the conjugate base for each compound below...Ch. 2.SE - 1, 1, 1-Trichloroethanol is an acid more than 1000...
Knowledge Booster
Background pattern image
Chemistry
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
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY