Module 4 - core organic chemistry Flashcards

1
Q

What is the general formula for all alcohols?

A

Cn H2n+1 OH

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2
Q

Define functional group

A

Group of atoms in a molecule which is responsible for the reaction

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3
Q

What are the three main types of organic reactions

A

Substitution
Elimination
Addition

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4
Q

What are the three main organic reaction mechanisms

A

electrophile (likes electrons/negative charges)
nucleophile (like positive charges)
radical (unpaired electron, ver aggressive)

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5
Q

What are electrophiles

A

electron pair acceptors

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6
Q

what are nucleophiles

A

electron pair donors

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7
Q

define hydrolysis

A

breaking of covalent bonds by reaction with water

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8
Q

define condensation

A

reaction in which two molecules combine to form a larger one and in which water or anoter small molecule is formed (lost)

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9
Q

Define alkanes

A

saturated hydrocarbons

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10
Q

What is the formula for alkanes?

A

CnH2n+2

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11
Q

Why do branched isomers have lower boiling points than unbranched?

A

less surface area of contact
weaker london forces
less energy required to overcome london forces

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12
Q

Define homolgues series

A

group of compounds with the same general formula but a different fuctional group
Differ by a CH2 group

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13
Q

Define aliphatic

A

a hydrocarbon joined together in straight chains, branched chains or non aromatic rings

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14
Q

Define alicyclic

A

an aliphatic compound containing a benzene ring

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15
Q

Define cycloalkane

A

a cyclic alkane e.g. cyclohexane

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16
Q

Define radical

A

species with an unpaired electron

17
Q

Define homolytic fission

A

each atom receives one bond electron, radicals are formed

18
Q

Define heterolytic fission

A

one atom receives both bond electrons, ions are formed

19
Q

What do full headed curly arrows show?

A

Movement of a pair of electrons

20
Q

What do half headed arrows show?

A

movement of a single electron

21
Q

Define alkene

A

Unsaturated hydrocarbons

22
Q

What is the general formula for alkenes?

23
Q

How are alkenes prepared?

A

from alcohols by elimination reaction or from crude oil

24
Q

What do double bonds have that make them a good target for electrophillic addition?

A

High electron density

25
What do halogen atoms bind to?
carbons from the double bond
26
What is the test for alkenes?
shake with bromine water at room temperature goes from orange to colourless
27
Describe bonding in alkanes
all four carbon bonds are sigma bonds the orbitals overlap in just one point and can therefore rotate across axis high bond enthalpy tetrahedral
28
Describe bonding in alkenes
double bond consists of one sigma and one Pi bond In the pi bond the P orbitals of two carbons overlap in two points (sideways) so they cannot rotate double bonds are stronger and shorter than single bonds high electron density trigonal planar
29
Define polymer
Long chain molecules of monomers
30
What are the rules of polymers
draw square bracket through the middle of the bond polymer chain is built is built only from carbons with a double bond - all other carbons form side chains remember to put n on both sides of the equation
31
Define structural isomer
same molecular formula but different structural formula
32
What are some characteristics of alcohols
high boiling points due to hydrogen bonds C-O bond polar OH good leaving group likes to undergo elimination and nucleophillic substitution reactions acts as a nucleophile in esterifcation reactions
33
What is the role of ozone
absorbs high energy UV radiation which causes skin cancer
34
What is indicated by a higher boiling point than expected?
impurities