Alkanes Flashcards

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1
Q

How can larger molecules minimise their cloud interactions?

A

Rotation occurs around carbon-carbon single bonds to also minimise electron cloud interactions.

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2
Q

What are the different spatial arrangements of the atoms that result from the rotation around the sigma carbon-carbon bonds called?

A

Conformations.

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3
Q

What are conformations?

A

The different spatial arrangements of the atoms that result from the rotation around the sigma Carbon-Carbon bond.

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4
Q

What is a sawhorse representation?

A

A 3D representation of a molecule showing bonds

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5
Q

What is a Newman projection?

A

A front-on view of the molecule, particularly of linear carbon chains, which will block the view of chain carbons, but show the arrangement of the branched chains.

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6
Q

What is eclipsed conformation?

A

When the adjacent hydrogens are in line with each other (rather than separated at 60 degree angles)

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7
Q

What is staggered conformation?

A

When the adjacent hydrogens are separated at a 60 degree angle.

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8
Q

Which is the highest energy formation: eclipsed or staggered?

A

Eclipsed

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9
Q

Which is the lowest energy formation: eclipsed or staggered?

A

Staggered

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10
Q

Which is the most stable formation: eclipsed or staggered?

A

Staggered

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11
Q

Which is the least stable formation: eclipsed or staggered?

A

Eclipsed

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12
Q

What is steric strain?

A

The strain experienced by a molecule when groups are too close to one another causing their electron clouds to repel each other.

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13
Q

What is steric strain also called?

A

Hinderance

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14
Q

Why do organic chains tend to take a linear formation?

A

Any other orientation will result in atoms being close together, giving more steric strain and making the molecule less stable.

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15
Q

If a conformation of a molecule is offset, but is not the most favourable, what is it called?

A

Gauche.

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16
Q

What is the relationship between steric strain and stability?

A

Steric Strain decreases stability

17
Q

What do single bonds allow for in terms of the shape of a molecule?

A

Carbon-Carbon bond rotation allows the peptide to twist. How much or how little it twists is controlled by steric strain.

18
Q

What can flexible bonds do?

A

Rotate about single bonds.

19
Q

What are flexible molecules called?

A

Rotamers

20
Q

What is it called as a molecule rotates through bonds?

A

Conformational change

21
Q

What is a limitation of the stick-and-ball atom figures you make in science classes?

A

They are inaccurate because in truth the atoms are much, much closer than that (to scale)

22
Q

What is done to represent the carbon(s) you can’t see in a Newman Projection?

A

A circle is drawn around the front carbon.

23
Q

For the back carbon(s) in a Newman projection, where do you draw the lines from?

A

The circle, not the point.

24
Q

If you have a molecule with carbon branches extending from the main chain, how do you make it staggered?

A

The carbon chains must be opposite.