ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
12th Edition
ISBN: 9781119664635
Author: Solomons
Publisher: WILEY
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Chapter 5, Problem 18PP
Interpretation Introduction

Interpretation:

The configuration (R,S) is to be assigned at each chirality center in Darvon.

Concept Introduction:

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

▸ A pair of two mirror images which are non-identical is known as enantiomers which are optically active.

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

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

▸ The stereoisomers which are non-superimposable on each other and not mirror images of each other are known as diastereomers.

▸ Chiral molecules are capable of rotating plane polarized light

▸ The molecules which are superimposable or identical with their mirror images are known as achiral molecules, and achiral molecules are not capable of rotating the plane-polarised light.

▸ Priority is given to all the four group attached to the chirality center.

▸ Priority is assigned according to the atomic number of the atom. Higher the atomic number, higher the priority given.

▸ If priority cannot be assigned according to atomic mass, then assign the priority according to the first point of difference.

▸ After giving priority to the four groups, rotate the molecule such that the fourth priority group is away from the observer.

▸ Now, move from a to b to c; if the direction is clockwise, then the chiral center is designated as (R) and if the direction is anticlockwise, then the chiral center is designated as (S).

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f) The unusual molecule [2.2.2] propellane is pictured. 1) Given the bond length and bond angles in the image, what hybridization scheme best describes the carbons marked by the askerisks? 2) What types of orbitals are used in the bond between the two carbons marked by the askerisks? 3) How does this bond compare to an ordinary carbon-carbon bond (which is usually 1.54 Å long)? CH2 1.60Å H₂C * H₂C CH2 C H2C * C Of H₂ 120°
e) Determine the hybridization and geometry around the indicated carbon atoms. H3C CH3 B HC CH2 A C C C CH3
Don't used Ai solution and hand raiting

Chapter 5 Solutions

ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT

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