Module 4 Flashcards

(41 cards)

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

25
what happens in initiation
covalent bond in a halogen molecule is broken by homolytic fission and 2 radicals are formed
26
what happens in propogation
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
what happens in termination
2 radicals collide forming a molecule with all electrons paired
28
limitations of radical sub
further substitution substitution at different positions in a carbon chain
29
structure of alkenes
unsaturated hydrocarbons pi bond which locks the 2 carbon atoms in position and prevents rotation
30
whats a pi bond
the sideways overlap of 2 p orbitals above and below the carbon atoms
31
conditions for E/Z isomerism
c=c different groups attached to each carbon atom of the double bond
32
Z isomerism
both priority groups are on the same side of the double bond
33
E isomerism
the priority groups are on different side of the double bond
34
priority groups in isomerism
the higher the atomic number the higher the priority
35
cis/trans isomer
one of the attached groups on each carbon atom of the double bond must be the same
36
cis isomer
baso same as z isomer , both groups on the same side
37
trans isomer
baso same as a E isomer , groups on opposite side of the double bond
38
reactivity of alkene
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
hydrogenation of alkenes
h2 and a nickel catalyst at 423k
40
halogenation of alkenes
at rtp with a halogen
41
testing for unsaturation
add bromine water to solution , if theres a double bond the solution turns colourless