Organic Flashcards

1
Q

what is stronger, hydrogen bonding, dipole dipole or London dispersion forces

A

hydrogen bonding > dipole/dipole > London

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2
Q

what are the solvency laws

A

like dissolves like
polar dissolves ionic

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3
Q

is O==H polar or non-polar

A

polar because O takes the electrons

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4
Q

what is electrophilic addition

A

In organic chemistry, an electrophilic addition reaction is an addition reaction where a chemical compound containing a double or triple bond has a π bond broken, with the formation of two new σ bonds.

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5
Q

what is markovnikov’s rule

A

new H goes to side with many Hs

the electronegative element will bond to the carbon with more groups

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6
Q

what is more stable - a primary or secondary carbocation

A

secondary (more electrons can be given)

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7
Q

can you sub a H attached to a C

A

no, need an O or N

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8
Q

can C have >4 bonds

A

no

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9
Q

what happens when a haloalkane reacts with NaOH

what will the product be

A

the OH will replace the halogens bond & the Na would attach with the halogen

product will be alcohol

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10
Q

in Markovnikov’s rule where does the H attach

A

the side with the least Hs

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11
Q

in Markovnikov’s rule where does the hydroxl group attach

A

the side with more hydroxl groups

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12
Q

what is oxidation

A

the loss of H and gain of O

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13
Q

how do primary alcohols oxidise

A

alcohol==> aldehyde group ==> carboxylic group e.g.

C–C==O & H attached to middle C = C–C==O and OH attached to middle C

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14
Q

can you oxidise a tertiary alcohol

A

no

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15
Q

what is esterification

A

alcohol + carboxylic acid

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16
Q

what is an amide

A

amine group (NH2) + carboxylic

17
Q

what is a major reaction vs a minor reaction

A

on a major reaction, the haloalkane will attach following markovnikov’s rule e.g. H to side with less Hs, Br to attach double bond. For minor products it will be the opposite way around

18
Q

how many Hs are needed for each C==C (carbon double bond)

A

2

19
Q

what is a primary alcohol group & what is it’s product process

A

an OH with one C attached e.g. on the end of the chain

  1. lose 2 H’s become aldehyde
  2. add O, become carboxylic acid
20
Q

what is a secondary alcohol group

A

2 carbons attached (probably in the middle)

  1. lose 2 H’s become ketone
  2. no more reaction
21
Q

can the tertiary alcohol group oxidise

A

no, no reaction