Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 7, Problem 7.1P
Interpretation Introduction

Interpretation:

The electron-poor H atom in methanol is to be identified, and the mechanism by which methanol acts as an acid in a proton transfer reaction with H2N is to be drawn.

Concept introduction:

An electron poor atom or a molecule is an atom or a site in a molecule that has fewer electrons than the number required for stability. In a proton transfer reaction, a proton is transferred from a Bronsted-Lowry acid (proton donor) to a Bronsted–Lowry base (proton acceptor). In an elementary step, electrons tend to flow from an electron-rich site to an electron-poor site. The curved arrow notation shows the movement of valence electrons.

Expert Solution & Answer
Check Mark

Answer to Problem 7.1P

The electron-poor H atom in methanol is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.1P , additional homework tip  1

The mechanism by which methanol acts as an acid in a proton transfer reaction with H2N is:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.1P , additional homework tip  2

Explanation of Solution

Atoms in CH3OH do not bear full charge. However, the high electronegativity of oxygen leads to a partial positive charge on the H to which it is bonded. Therefore, H is electron poor. H2N bears full negative charge, and therefore, it is electron rich. The curved arrow from a lone pair on N to the H atom on O represents the flow of electrons from the electron-rich site (H2N) to the electron-poor site (CH3OH). A second curved arrow is needed to make sure H has only one bond, not two.

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 7, Problem 7.1P , additional homework tip  3

Conclusion

The curved arrows are drawn from the electron-rich site (H2N) to the electron-poor site (CH3OH).

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
reciprocal lattices rotates along with the real space lattices of the crystal. true or false?
Deducing the reactants of a Diels-Alder reaction vn the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ O If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Click and drag to start drawing a structure. Product can't be made in one step. Explanation Check
Predict the major products of the following organic reaction: Δ ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. L

Chapter 7 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

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 for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Text book image
Pushing Electrons
Chemistry
ISBN:9781133951889
Author:Weeks, Daniel P.
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
How to Design a Total Synthesis; Author: Chemistry Unleashed;https://www.youtube.com/watch?v=9jRfAJJO7mM;License: Standard YouTube License, CC-BY