(YELLOW) ISOMERISM Flashcards

(YELLOW) ISOMERISM

1
Q

what is the definition of an structural isomer

A

Structural isomers are compounds that have the same molecular formula but different structural formula (i.e. different bonds present)

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2
Q

what are the three types of structural isomers and what do they do

A

Type 1. Chain structural isomers. : same molecular formula but diffrent structure

Type 2 Positional structural isomers. : basically functional group in a diffrent place

Type 3. Functional group structural isomers : same molecular formula bust diffrent functional group . e.g carboxilic group / ketone

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3
Q

what is the definition of a steroisoerism

A

Stereoisomerism is shown in molecules that have the same molecular formula and same bonds present, but different three dimensional orientations of their atoms in space.

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4
Q

what is geometrical isomerism

A

when you have an alkene the two carbons with the double bond have to have each two diffrent groups on them , thererfor causing z/e isomers / cis / trans isomers

must have C=C bond

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5
Q

can cyclic compounds show geometric isomerism

A

yes as the ring structure can cause restriction

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6
Q

What is a superimposable mirror image of each other?

A

it means that its mirror image cannot be destinguished

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7
Q

what is a chiral carbon

A

One way to identify an optical isomer is to find a carbon with 4 different groups attached to it. We call this carbon a chiral carbon or chiral centre. If the molecule has a chiral centre is will be asymmetric and therefore have optical isomers.

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7
Q

what is the definition of an optical isomer

A

Optical isomers (enantiomers) are molecules which are isomers which are non-superimposable mirror images of each other.

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8
Q

what featur of optical isomers does it show with light

A

Optical isomers ROTATE the plane of plane polarised light. Each isomer will rotate the light by the same amount but in the opposite direction.

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9
Q

waht is a racemic misture

A

A Racemic mixture is a solution which contains equal numbers of moles (concentrations) of both optically active isomers/enantiomers of a compound.

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10
Q

Would you expect a racemic mixture to be optically active/rotate plane polarised light?

Explain your answer.

A

NO

A racemic mixture contains two optical isomers / enantiomers in equimolar quantities.

One isomer rotates the plane of plane polarised light in one direction, the other isomer rotates it in an equal and opposite direction so the rotations cancel out resulting in no overall rotation of plane polarised light

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11
Q

what are optical isomers called

A

enantiomers

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12
Q

true or false :
Racemates contain 2 enantiomers in equal numbers

A

true

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13
Q

true or false :
The synthesis of a single optical isomer, rather than racemates, is less expensive

A

false

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14
Q

true or false :
Chiral molecules produced naturally by enzymes are usually a racemic mixture

A

false

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15
Q

true or false :
Two enantiomers have identical properties when taken as medicines

A

flase

16
Q

true or false :
If two enantiomers have different effects on the human body, one will be inactive

and do nothing

A

flase

17
Q

true or false :
Chiral drugs which are administered as only one enantiomer normally have

increased pharmacological effects and reduced side effects

A

true

18
Q

true or false :
Naturally occurring chiral molecules such as L amino acids may be used as

starting materials and molecular templates in the manufacture of a drug

A

true

19
Q

true or false :
Chiral catalysts may be used to help the reaction and also to confer chirality

A

true

20
Q

what type of group commonly undergoes SN1

A

2o or 3o

21
Q

what type of group commonly undergoes SN2

A

1o

22
Q

what is steric hinderance

A

large groups getting in the way of the attacking species

23
Q

how can SN1 or SN2 cause osptical isomers

A

SN1 causes a plainer tertiary structure so species can attack from top or bottom causing a racimic misture

SN2 species can only attack from one side so will form a optically active mixture