1. into to organic Flashcards

1
Q

empirical formula

A

simplest whole number ratio of atoms of an element in a compound

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2
Q

molecular formula

A

the actual number of each atom of an element in a compound

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3
Q

structural formula

A

minimal detail showing arrangement of atoms in a molecule

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4
Q

displayed formula

A

all the atoms and cov. bonds present in a molecule

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5
Q

skeletal formula

A

simplified organic formula showing on carbon skeleton and functional groups

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6
Q

side groups

A

alkyl groups branching off the main c chain. you need numbers to indicate the position

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7
Q

homologous series

A

a series of compounds containing the same functional group. they have:
- the same chemical properties and
- a trend in physical properties
- they increase by a ch2 group every time
- they have the same gen formula

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8
Q

functional group of
alkenes
alcohols
haloalkanes
aldehydes

A

C=C

C-OH

C-X

C=O and a H on the C too lol (in formula it’s CHO

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9
Q

functional group of
ketones
c acids
nitriles
amines

A

C=O

COOH

C triple bond N

C-NH2

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10
Q

priority order for naming when there’s >1 f group

A

c acids
aldehyde
ketones
alcohols
alkenes
haloalkanes

f group with higher precedence takes the suffix and the lowest C in chain.

if an alkene was also with a c acid since c acid takes suffix it becomes eg butenoic acid (-en-)

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11
Q

if the suffix (f group) begins with a vowel then

A

take the e off stem alkane

eg butane alcohol
butanol

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12
Q

if suffix starts w consonant (give eg) then

A

keep the -e on the alkane stem

dioic acid
nitrile
diol

eg hexane diol
hexane-2,3-diol

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13
Q

structural isomerism

3 types

A

same molecular formula but different structural formula

  • chain
  • position
  • f group
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14
Q

chain isomerism

A

same m formula diff structures of c skeleton / chain length

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15
Q

position isomerism

A

same m formula different position of same f group on same c skeleton

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16
Q

functional group isomerism

A

same m formula, atoms arranged into diff f groups

17
Q

isomerism -> structural (chain, f group, position) // stereoisomerism

2 types

A

same m/s formula different 3d spatial arrangements of atoms

geometric + (optical but that’s a level)

optical - molecules have the same molecular
formula but a different spatial arrangement of atoms in space. It occurs when there is an
asymmetrical carbon within an organic molecule known as a chiral centre. Chiral carbons have four different groups bonded to them

18
Q

what effect can geometric stereoisomerism have

A

on physical properties bc molecule can be polar or not due to the atomic arrangement. so could have D-D IMF making forces maintaining m/BP higher

19
Q

f group structural isomerism pairs

A

alkenes and cycloalkanes

aldehydes and ketones

alcohols and ethers (f group R-O-R)

c acids and esters (f group r-c double bond o, o-r)

20
Q

what f group shows geometric isomerism? why?

A

alkenes that have 2 diff atom groups on each C

C=C has limited rotation so atoms are arranged differently in space

21
Q

how is an isomer E or Z

how determine this?

A

priority groups are opposite for E , on the same side for Z

determine using cahn-ingold-prelog rules:
1. look at atomic numbers on atoms attached to C in C=C
2. you’re comparing groups on same C against eachother
3. no totalling
4. winner gets priority 1
5. priority 1s on same side -> Z

22
Q

reactions of organic compounds can be explained using

A

mechanisms