Module 4 Flashcards

1
Q

whats a hydrocarbon

A

a compound containing carbon and hydrogen only

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2
Q

saturated hydrocarbon

A

has single bonds only

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3
Q

unsaturated hydrocarbon

A

contains double or triple bonds

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4
Q

homologous definition

A

a family of compounds with similar properties whose successive members differ by the addition of a CH2 group

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5
Q

whats a functional group

A

the part of the organic molecule that is largely responsible for the molecules chemical properties

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6
Q

aliphatic definition

A

carbon atoms are joined to each other in unbranched or branched chains or non aromatic rings

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7
Q

alicyclic definition

A

carbon atoms are joined to each other in ring structure with or without branches

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8
Q

aromatic definition

A

some or all of the carbon atoms are found in a benzene ring

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9
Q

alkynes

A

contain a triple bond

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10
Q

empirical formula

A

is the simplest whole number ratio of the atoms of each element present in a compound

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11
Q

general formula

A

the simplest algebraic formula for any member of a homologous series

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12
Q

molecular formula

A

shows the number and type of atoms of each element present in a molecule

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13
Q

structural isomerism

A

compounds with the same molecular formula but different structural formulae

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14
Q

homolytic fission

A

each of the bonded atoms takes one of the shared pair of electrons from the bond

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15
Q

radical definition

A

an atoms or group of atoms with an unpaired electrons

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16
Q

heterolytic fission

A

when a covalent bond breaks one of the atoms takes both the electrons from the bond

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17
Q

curly arrows

A

show the movement of a pair of electrons

18
Q

the bonding in alkanes

A

only contain single bonds (saturated)
sigma bonds

19
Q

shape of alkanes

A

tetrahedral arrangement around each carbon atoms with a bond angle of 109.5

20
Q

boiling points in alkanes

A

as the chain length increases so does the boiling point as london forces act between molecules that are in close surface contact so as chain length increases the molecules have a larger surface area with more surfaace contact between molecules , so london forces will be greater

21
Q

affects of branching on boiling point of alkanes

A

branched isomers have lower boiling points as there will be fewer surface contact between molecules of the branched alkanes giving fewer london forces

22
Q

reactivity of alkanes

A

do not react with most common reagents because:
c-c and c-h sigma bonds are strong
c-c bonds are non-polar
c-h electronegativity is similar so baso non polar

23
Q

alkanes + halogens mechanism name

A

free radical substitution

24
Q

conditions for free radical sub

A

uv light

25
Q

what happens in initiation

A

covalent bond in a halogen molecule is broken by homolytic fission and 2 radicals are formed

26
Q

what happens in propogation

A

usually 2 steps where a halogen radical is reacting with an CH4 (as an example) to form CH3 and a hydrogen halide, this CH3 radical then reacts with eg br2 to from CH3Br and a br radical to react again with CH4

27
Q

what happens in termination

A

2 radicals collide forming a molecule with all electrons paired

28
Q

limitations of radical sub

A

further substitution
substitution at different positions in a carbon chain

29
Q

structure of alkenes

A

unsaturated hydrocarbons
pi bond which locks the 2 carbon atoms in position and prevents rotation

30
Q

whats a pi bond

A

the sideways overlap of 2 p orbitals above and below the carbon atoms

31
Q

conditions for E/Z isomerism

A

c=c
different groups attached to each carbon atom of the double bond

32
Q

Z isomerism

A

both priority groups are on the same side of the double bond

33
Q

E isomerism

A

the priority groups are on different side of the double bond

34
Q

priority groups in isomerism

A

the higher the atomic number the higher the priority

35
Q

cis/trans isomer

A

one of the attached groups on each carbon atom of the double bond must be the same

36
Q

cis isomer

A

baso same as z isomer , both groups on the same side

37
Q

trans isomer

A

baso same as a E isomer , groups on opposite side of the double bond

38
Q

reactivity of alkene

A

more reactive than alkanes because of the presence of the pi bond which as an electron dense area and so alkenes undergo addition reactions quite easily

39
Q

hydrogenation of alkenes

A

h2 and a nickel catalyst at 423k

40
Q

halogenation of alkenes

A

at rtp with a halogen

41
Q

testing for unsaturation

A

add bromine water to solution , if theres a double bond the solution turns colourless