UNIT 4 Flashcards
STEREOISOMERISM
DEFINE STEREOISOMERISM
SAME MOLECULAR FORMULA BUT ATOMS OCCUPY DIFFERENT SPACIAL ARRANGEMENT
STEREOISOMERISM
WHAT ARE THE TWO TYPES OF STEREOISOMERIS
GEOMETRICAL AND OPTICAL
STEREOISOMERISM
HOW DOES GEOMETRICAL ISOMERISM OCCUR
DUE TO C=C BONDS THERE IS RESTRICTED ROTATION.
FORMS ‘E’ AND ‘Z’ ISOMERS
STEREOISOMERISM
HOW DOES OPTICAL ISOMERISM OCCUR
OCCURS WHEN MOECULES HAVE A CHIRAL CENTRE.
GET TWO NON-SUPERIMPOSABLE MIRROR IMAGES
HOW IS STERIOISOMERISM DIFFERENT TO STRUCTURAL ISOMERISM
STRUCTURAL ISOMERISM= SAME MOLECULAR FORMULA BUT DIFFERENT STRUCTURAL FORMULAE
STEREOISOMERISM= SAME MOLECULAR FORMULA BUT ATTOMS OCCUPY DIFFERENT POSITIONS IN SPACE
STEREOISOMERISM
THREE TYPES OF STRUCTURAL ISOMERISM
CHAIN ISOMERISM , POSITIONAL ISOMERISM , FUNCTIONAL GROUP ISOMERISM
when does optical isomerism form
same molecular formula but different spacial arrangement
occurs when there is a asymetrical carbon chiral centre in a molecule.
what are two optical isomers calleled
encantomers
HOW TO DIFFERENTIATE BETWEEN ENCANTOMERS
SHINE PLANE POLARISED LIGHT ON THEM
EACH ENCANTMER WILL CAUSE THE LIGHT TO ROTATE 90 DEGREES DEPENDING ON WHETHER ITS A LHS OR A RHS ENCANTOMER.
EXPLAIN NUCLEOPHILLIC ADDITION IN TERMS OF ECANTOMERS
NUCLEOPHILE CAN ATTACK CARBONYL GROUP FROM ABOVE OR BELOW. CAUSING TWO MIRROR IMAGES OF A TRIGONAL PLANAR MOLECULE TO FORM
DEFINE A RACEMIC MIXTURE
EQUAL AMOUNT OF EACH ENCANTOMER FORMED.
NO OVERALL EFFECT AS IT IS EQUAL.
DEFINE A RACEMIC MIXTURE
EQUIMOLAR MIXTURE OF EACH ENCANTOMER FORMED.
NO OVERALL EFFECT AS IT IS EQUAL.
ALCOHOLS
GENERAL FORMULA
FUNCTIONAL GROUP
CnH2n OH
-OH FUNCTIONAL GROUP
PRIMARY ALCOHOLS
-OH GROUP ATTATCHED TO ONLY ONE CARBON ATOM AND ONLY ONE METHYL GROUP IS ATTATCHED
TEST FOR PRIMARY ALCOHOLS
CAN BE OXIDISED TO FORM ALDEYDES WHICH CAN BE OXIDISED FURTHER TO FORM CARBOXYLIC ACIDS