number 1 Flashcards

(16 cards)

1
Q

What are constitutional isomers?

A

Compounds with the same molecular formula but different connectivity

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2
Q

Give an example of constitutional isomers of C2H6O.

A

Ethanol and dimethyl ether

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3
Q

Do constitutional isomers have different properties?

A

Yes they have completely different physical and chemical properties

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4
Q

What is stereoisomerism?

A

Isomers with the same connectivity but different 3D arrangement

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5
Q

Why is stereochemistry important in pharmacy?

A

Many drugs require correct stereochemistry for safety and efficacy

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6
Q

Name the three main types of stereoisomerism.

A

Conformational optical and geometrical

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7
Q

What are conformational isomers?

A

Isomers formed by rotation around single bonds

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8
Q

Which conformer of ethane is most stable?

A

The staggered conformer

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9
Q

Why is staggered ethane lower in energy?

A

Hydrogens are as far apart as possible reducing repulsion

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10
Q

What is torsional strain?

A

Energy increase due to eclipsing bonds

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11
Q

What is torsional energy?

A

Energy needed to rotate from staggered to eclipsed

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12
Q

Which conformation of butane is most stable?

A

The anti conformation

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13
Q

Which conformation of butane is least stable?

A

The fully eclipsed conformation

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14
Q

Why is anti-butane most stable?

A

Methyl groups are maximally separated

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15
Q

Why is cyclopropane strained?

A

Bond angles are 60� instead of 109�

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16
Q

Why is cyclobutane puckered?

A

To reduce torsional strain between eclipsed hydrogens