Lesson 6 Flashcards

1
Q

The most Stable Alicyclic isomers

A

Staggered

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2
Q

The least stable alicyclic isomers

A

Eclipsed

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2
Q

How to calculate the bond angle

A

180 - 360/n

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3
Q

What happens when all H atoms are eclipsed

A

there will be a steric effect and the isomer becomes unstable

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4
Q

What happens when angle are stable

A

decrease in orbital overlap
C-C bond weakens
Good overlap
decrease overlap

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5
Q

True or False: the planar isomer of a cycloalkane is stable

A

False, planar isomers are unstable since cycloalkanes are typically not flat

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6
Q

True or False: Cyclopropane is always planar

A

true

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7
Q

Most stable conformation of Cyclobutane

A

fourth carbon is below to move away from eclipsed conformation

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8
Q

Most stable conformation of cyclopentane

A

Puckered envelope conformation, where fifth carbon does not lie on the same plane

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9
Q

Most stable conformation of cyclohexane

A

Chair conformation

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10
Q

Least stable conformation of cylcohexane

A

Half chair, since it has the higehst energy

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11
Q

Are chair isomers the same compound?

A

yes, since it is simply interconvertible through the ring flip

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12
Q

Can chair isomers be separated in the lab?

A

No, since they are the same compound with the same chemical and physical properties, there is no way to separate the isomers

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13
Q

True or False: Axial is more stable than equatorial

A

False, Axial makes substituent parallel to hydrogen which leads to steric strain

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14
Q

True or False: Cis and trans isomers are the same compound

A

False, they are different compounds since they are not interconvertible

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15
Q

Where are cis and trans applicable

A

applied to double bonds
alicyclic structures

16
Q

How to know if there are optical isomers

A

if it has non-superimposable mirror images