Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
bartleby

Concept explainers

bartleby

Videos

Textbook Question
Book Icon
Chapter 14, Problem 24P

(a) In 1960 T. Katz (Columbia University) showed that cyclooctatetraene adds two electrons when treated with potassium metal and forms a stable, planar dianion, C 8 H 8 2 (as the dipotassium salt):

Chapter 14, Problem 24P, 14.24	(a)	In 1960 T. Katz (Columbia University) showed that cyclooctatetraene adds two electrons , example  1

Use the molecular orbital diagram given in Fig. 14.7 and explain this result.

(b) In 1964 Katz also showed that removing two protons from the compound below (using butyllithium as the base) leads to the forma-tion of a stable dianion with the formula C 8 H 6 2 (as the dilithium salt).

Chapter 14, Problem 24P, 14.24	(a)	In 1960 T. Katz (Columbia University) showed that cyclooctatetraene adds two electrons , example  2

Propose a reasonable structure for the product and explain why it is stable.

Blurred answer
Students have asked these similar questions
(b) Answer BOTH parts (i) and (ii). (i) Using your knowledge of silicon chemistry, explain why the synthesis of a compound containing a formal Si=0 double bond is challenging. (ii)Bearing in mind your answer to part (i), suggest a synthetic route to a silanone, R2Si=O, starting from silicon tetrachloride SiCl4 and using any other reagents you choose. Identify all reagents and side-products in your synthetic route and specify your chosen R group, giving reasons for your choice.
Write the equilibrium-constant expressions and obtain numerical values for each constant in             (a) the basic dissociation of aniline, C6H5NH2.             (b) the acidic dissociation of hypochlorous acid, HClO.             (c) the acidic dissociation of methyl ammonium hydrochloride, CH3NH3Cl.             (d) the basic dissociation of NaNO2.             (e) the dissociation of H3AsO3 to H3O+ and AsO33- just answer the letters C, D and E.
Give reasons for the following :(i) Phenol is more acidic than methanol.(ii) The C—O—H bond angle in alcohols is slightly less than the tetrahedral angle (190°28′).(iii) (CH3)3C—O—CH3 on reaction with HI gives (CH3)3C—I and CH3—OH as the main products and not (CH3)3C—OH and CH3—I.

Chapter 14 Solutions

Organic Chemistry

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
Molecular spectroscopy; Author: Vidya-mitra;https://www.youtube.com/watch?v=G6HjLIWvCQo;License: Standard YouTube License, CC-BY