Alkanes + Cyclo Flashcards

1
Q

According to old names a propane substituent bonded at the middle is called what?

A

Isopropyl

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2
Q

What is a primary carbon?

A

One which is bonded to 1 other carbon

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3
Q

What is a secondary carbon?

A

One which is bonded to 2 other carbons

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4
Q

What is a tertiary carbon?

A

One which is bonded to 3 other carbons

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5
Q

What happens to melting/ Boiling points as the carbon chain gets longer and why?

A

They increase due to stronger London dispersion forces

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6
Q

What are London dispersion forces?

A

When electrons repel each other creating temporary delta positives and negatives, thus a temporary dipole.
Theyre really weak intermolecular interactions

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7
Q

Do branched alkanes have higher or lower melting boiling points than straight chains?

A

Lower, they’re harder to pack and therefore experience less temporary dipoles (London dispersion forces)

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8
Q

Are alkanes reactive?

A

Quite unreactive due to strong c-c

But can have reactions eg with chlorine gas and can be burnt (oxidisation)

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9
Q

Why do we burn alkanes?

A

The c-c bond is really strong, so when burnt it releases a lot of energy which can be used.

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10
Q

What is a constitutional isomer?

A

It has a different structural arrangement, different connectivity

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11
Q

What is an molecule isomer?

A

Different molecules that have the same molecular formula. So can be arranged differently etc

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12
Q

What does a staggered conformation mean?

A

When atoms are in the form with lowest energy. they face the least repulsion, atoms are as far apart as possible within the molecule

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13
Q

What does an eclipsed conformation mean?

A

Molecule has rotated in a way in which atoms are overlapping. Electrons repel each other therefore this form is a high energy form

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14
Q

What is the anti conformation?

A

When the molecule has rotated in a way in which no atoms are overlapping, it has the least repulsion between atoms and is therefore the most stable

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15
Q

What is the gauche conformation?

A

When the molecule has rotated in such a way that it is staggered but there may be some groups overlapping so it is higher in energy than the anti conformation

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16
Q

How can molecules have rigidity if they are constantly rotating? (eg enzymes)

A

By creating ring structures, bond ability to rotate is significantly decreased

17
Q

Why are many enzymes cyclic?

A

Cyclic bonds are harder to rotate and are therefore more rigid

18
Q

Are cycloalkanes isomers of the linear version?

A

No there is normally two less hydrogens, different molecular formula

19
Q

Why are 6 membered rings the most common?

A

They experience the least ring strain.

20
Q

What is torsional strain?

A

strain in a ring caused by trying to avoid eclipsing. (ring puckers)

21
Q

What is steric ring strain?

A

When the bulkiness of the groups causes them to be close

22
Q

What is angle strain?

A

When the ring forms angles that deviate from the common carbon tetrahedral 109.5 degrees

23
Q

What has lower energy the boat or the chair conformation? and why?

A

Chair has lower energy as the atoms are more staggered, they face less repulsion and are therefore more stable

24
Q

Why does boat conformation have higher energy than chair?

A

It has more torsional strain. Groups closer together

25
Q

What is lower in energy equatorial position or axial?

A

equatorial as it can be further from other atoms

26
Q

Why do most rings once in chair conformation normally stay in chair?

A

It is the lowest energy form, also the energy cost to get to half chair form is really high

27
Q

What is thermodynamically more stable, CIS or TRANS?

A

Trans as they are on opposite sides, therefor face less repulsion

28
Q

What kind of isomers are cis and trans?

A

Stereoisomers

29
Q

What is a stereoisomer?

A

orientation in space is different. Put together in the same way.

30
Q

What is a constitutional isomer?

A

Same molecular formula but different connectivity

31
Q

with a longer chain of alkane is it more or less likely to be solid?

A

More likely since more intermolecular forces (London dispersion forces)

32
Q

What is electronegativity?

A

How good it is at pulling electrons towards itself

33
Q

Order of strength of forces

A
Covalent
ionic
hydrogen
dipole-dipole
induced-dipole
induced-induced (London)
34
Q

Do branched or linear alkanes have higher melting points?

A

Linear have higher melting points since they can pack better so more intermolecular forces

35
Q

Why do spontaneous reactions happen?

A

products are more stable than reactants so more energy given out then needed to break or make the bonds