ORGANIC CHEM LL W/WILEYPLUS BLCKBRD >I
ORGANIC CHEM LL W/WILEYPLUS BLCKBRD >I
12th Edition
ISBN: 9781119238249
Author: Solomons
Publisher: WILEY
bartleby

Concept explainers

Question
Book Icon
Chapter 5, Problem 20PP
Interpretation Introduction

Interpretation:

The optically active compounds among the given compounds are to be identified.

Concept introduction:

The molecules that are non-superimposable or not identical with their mirror images are known as chiral molecules.

A pair of two mirror images that are non-identical is known as a pair of enantiomers, and these are optically active.

The enantiomers in which the path traced from the highest to the lowest atomic number is in the anticlockwise direction are designated as S provided that among the four groups attached to the chiral carbon, the least priority group is in horizontal position in Fischer projection.

The enantiomers in which the path traced from the highest to the lowest atomic number is in the clockwise direction are designated as R provided that among the four groups attached to the chiral carbon, the least priority group is in horizontal position in Fischer projection. .

The objects or molecules which are superimposable with their mirror images are achiral objects or molecules. These objects have a centre of symmetry or plane of symmetry.

The achiral compounds in which the plane of symmetry is present internally and consists of chiral centres are known as meso compounds, but they are optically inactive.

Blurred answer
Students have asked these similar questions
If either of the following molecules has a stereogenic carbon (chirality center), give structures for both of the enantiomers.               (a)  2-bromopropane                           (b) 2-bromobutane
(a) All Isomers have the same molecular formulae. Explain this further. Hint what does it mean to have the same molecular formulae? (b) What is Constitutional (structural) isomerism? Hint, isomers are different, so what is different between a pair of constitutional isomers (see the chart on the last page for examples). (c) What is Conformational isomerism?
5.76 2,3-Dibromoprop-1-ene (C3H4Br₂) has four H atoms. Suppose that any of these H atoms can be replaced by a Cl atom to yield a molecule with the formula C3H3Br₂Cl. (a) Identify two H atoms where this substitution would yield constitutional isomers of C3H3Br₂Cl; (b) enantiomers of C3H3Br₂Cl; (c) diastereomers of C3H3Br₂Cl. co 11 HHH Juods H Brugtrio 2 bas A 2,3-Dil so ontemme A chon Br 2,3-Dibromoprop-1-ene

Chapter 5 Solutions

ORGANIC CHEM LL W/WILEYPLUS BLCKBRD >I

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