hydrocarbons Flashcards

1
Q

organic compounds def

A

compounds that contain carbon atoms covalently bonded to atoms of other elements, usually hydrogen, oxygen, nitrogen or chlorine.

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2
Q

homologous series def

A

consists of a family of compounds with the same general formula, and similar chemical properties because they have the same functional group

–> gradual change of physical properties as a result of increase in size and mass of molecules

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3
Q

functional group def (for understanding)

A

atom or combination of atoms which gives organic molecules distinctive chemical properties

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4
Q

alkanes and functional group

A

carbon-carbon single bond (C–C)
general formula: CnH2n+2

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5
Q

alkenes and functional group

A

carbon-carbon double bond (C=C)
general formula: CnH2n

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6
Q

alcohol and functional group

A

hydroxyl (—O–H)
general formula: CnH(2n+1)OH

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7
Q

carboxylic acid and functional group

A

carboxyl O
||
—C–O–H
(–COOH)
general formula: C(n-1)H(2n-1) COOH

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8
Q

meth- prefix, carbon atoms = ?

A

1

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9
Q

eth- prefix, carbon atoms = ?

A

2

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10
Q

prop- prefix, carbon atoms = ?

A

3

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11
Q

but- prefix, carbon atoms = ?

A

4

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12
Q

–ane suffix, homologous series = ?

A

alkane

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13
Q

–ene suffix, homologous series = ?

A

alkene

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14
Q

–ol suffix, homologous series = ?

A

alcohol

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15
Q

–oic acid, homologous series = ?

A

carboxylic acid

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16
Q

alkanes def

A

hydrocarbons that contain only carbon-carbon single bonds and carbon-hydrogen bonds

obtained from fractional distillation of petroleum

17
Q

saturated meaning in terms of alkanes

A

molecule contains only carbon-carbon single bonds. each carbon atom is covalently bonded to four other atoms (single bonds) so no new atom can add to it anymore

18
Q

alkane solubility

A

insoluble in water but soluble in organic solvents like tetrachlormethane (CCl4)

can be used as solvents for other organic compounds (liquid hexane to alkenes)

19
Q

changes in physical properties as size and mass of alkane molecules increases down series

A
  1. melting point and boiling point increases
  2. density increases
  3. viscosity increases
  4. flammability decreases
20
Q

what happens to alkanes during COMPLETE combustion + equation

A

alkanes burn with blue flame without smoke

alkane + oxygen gas –> CO2 + H2O

21
Q

what happens to alkanes during INCOMPLETE combustion

A

alkanes burn with yellow smoky flame to produce products like soot (carbon), CO, H2O

alkane + oxygen –> C(s) + CO (g) + H2O [not always all three]

22
Q

catalyst for a substitution reaction

23
Q

what happens during a substitution reaction

A

a hydrogen atom is substituted to form chloromethane and hydrogen chloride is produced too

eg. methane (CH4 (g)) + chlorine (Cl2 (g)) -UV light-> chloromethane (CH3Cl (g)) + HCl (g)

more hydrogen atoms can be replaced to form products like dichloromethane

24
Q

alkenes def

A

hydrocarbons that contain carbon-carbon double (C=C) bonds

obtained from the cracking of alkanes

25
types of hydrocarbons of alkenes
unsaturated hydrocarbons; contains carbon-carbon double bonds, where each carbon atom is covalently bonded to three atoms only ratio of C:H atoms: 1:2
26
solubility of alkenes
insoluble in water but soluble in organic solvents like hexane and tetrachloromethane not used as solvents as they are reactive, so they can interfere with reactions
27
change of physical properties as size and mass of alkenes increases
1. boiling point increases 2. density increases 3. viscosity increases 4. flammability decreases
28
what happens during combustion of alkenes + eqn
burn with sootier flames than alkanes because the percentage of carbon by mass in alkenes is higher than that in alkanes for the same number of carbon atoms present in respective molecules alkene + oxygen gas --> CO2 + H2O
29
what happens during hydration of alkenes + eqn
1. pressure = 60 atm 2. temperature = 300 degree celsius 3. concentrated phosphoric (V) acid as a catalyst alkenes are converted to alcohol after addition of steam alkene + steam --> alcohol
30
what happens during hydrogenation
hydrogen is added to carbon-carbon double bond at high temperature and pressure to change to alkanes - nickel (transition metal) as catalyst alkene + hydrogen --> alkane
31
what happens during bromination
important test to distinguish alkanes from alkenes 1. alkene: bromine is decolourised 2. alkane: bromine remains brown, no reaction takes place
32
what is polymerisation
it is a process of joining small identical units to form large molecules with a high temperature and pressure and a catalyst
33
what is cracking
it is the breaking down of large alkane molecules to produce smaller useful molecules, with the use of high temperatures and pressures without a catalyst with a catalyst, it is catalytic cracking, which requires aluminium oxide or silicon dioxide as a catalyst, and a high temperature of about 500-700 degree celsius, and a pressure of 1 atm. two different pathways which lead to different product formation 1. large alkane --> mixture of alkenes + alkane 2. large alkane --> mixture of alkenes + hydrogen
34
isomer def
compounds that have the same molecular formulae but different structural formulae
35
straight chain vs branched chain of alkanes
straight: all carbon atoms connecting in a single continuous line branched: carbon atom(s) not connecting in a single continuous line and form a side chain known as alkyl group
36
alkyl group and their names
1. –CH3: methyl 2. –C2H5: ethyl 3. –C3H7: propyl
37
steps to naming isomers
1. look for the longest chain of carbon atoms (main chain), named according to number of carbon atoms 2. identify alkyl groups 3. indicate position of alkyl groups on the main chain. the position must be the lowest possible number