reactions Flashcards

(37 cards)

1
Q

reactant, condition and final product for substitution reaction

A

reactant: alkane + halogen
condition: under light
final product: haloalkane

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2
Q

why is light necessary for substitution reaction?

A

provide sufficient energy to break the Cl-Cl bonds in Cl2 molecules to form Cl radicals (where Cl can be Br or F(unlikely))

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3
Q

free radical definition & why it is highly reactive

A

definition: a particle that has at least one unpaired electron
unstable: it does not have a stable noble gas electronic arrangement/does not obey octet rule

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4
Q

what reaction will happen during propagation cycles? what is the definition of the reaction?

A

chain reaction; a sequence of reactions where a reactive product or by-product cause additional reactions to take place

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5
Q

observable changes when Br2 reacts with alkane under light

A
  1. orange bromine solution changes to colorless
  2. white fume is observed because of the formation of HBr
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6
Q

how is white fume formed during substitution reaction of alkanes with Br or Cl?

A

HBr/HCl formed dissolves in moisture in air to form acid droplets, which are seen as white fume

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7
Q

observable change when Cl2 reacts with alkane

A
  1. chlorine gas changes from yellow-green to colorless
  2. white fumes are formed due to the formation of HCl gas
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8
Q

what will be observed on a wet litmus paper if it is placed at the mouth of the test tube after substitution reaction of CH3 with Br?

A

the WET, not dry litmus paper will turn from blue to red

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9
Q

what will be observed on a dry litmus paper if it is placed at the mouth of the test tube after substitution reaction of CH3 with Br?

A

nothing its dry

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10
Q

what will be observed on a wet litmus paper if it is placed at the mouth of the test tube after substitution reaction of CH3 with Cl?

A

changes from blue to red as HCl gas is acidic –> ionizes in water; then changes to white as OCl- is a bleaching agent

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11
Q

rate of reaction (F2, Cl2, Br2, I2) with alkanes

A
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12
Q

major product for excess butane with chlorine

A

Excess alkane is monosubstitution so answer is C4H9Cl

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13
Q

when/where does cracking occur in the catalytic cracking set up?

A

when the vapour of alkane passes through the broken unglazed porcelain

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14
Q

catalyst used for catalytic cracking on an industrial scale

A

aluminium oxide or silicon dioxide

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15
Q

catalytic cracking in laboratory:
1. why heat broken unglazed porcelain strongly not only alkane? (2)
2. why broken?
3. why cannot remove delivery tube before heat source off?
4. what can replace broken unglazed porcelain?

A
  1. prevent alkane from vaporizing without reaction (1) if the surface of broken unglazed porcelain is not hot enough (1)
  2. increase surface area -> increase rate of reaction
  3. to prevent sucking back of water (1) sudden cooling may break boiling tube (1)
  4. broken pumice stone/broken porous pot/aluminium oxide (1)
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16
Q

importance of cracking in petroleum industry (2 reasons)

A
  1. to obtain smaller fractions which are of higher demand like petrol
  2. to obtain more alkenes which are important raw materials for chemicals (e.g. producing petrochemicals, plastics)
17
Q

explain from molecular level why petrol can be obtained from petroleum by fractional distillation (2 marks)

2014 dse q6a

A
  • different hydrocarbons in petroleum have different boiling points (1)
  • the longer the carbon chain, the higher the boiling point (1)
18
Q

other than directly obtaining petrol from fractional distillation of petroleum, suggest a way of producing extra petrol

A

cracking of heavy hydrocarbons

19
Q

explain why CH3Cl is not the only organic product formed in the reaction between CH3 and Cl

A

CH3 undergoes further substitution/polysubstitution to form CH2Cl2, CHCl3 and CCl4

20
Q

types of addition reactions (5 types)

A
  1. hydrogenation/catalytic hydrogenation
  2. reaction with cold acidified potassium permanganate solution
  3. halogenation
  4. hydrohalogenation
  5. addition polymerization
21
Q

definition of catalytic hydrogenation

A

conversion of unsaturated alkenes to saturated alkanes

22
Q

hydrogenation reaction formula

A

–C=C– + H2 — (Pt, Pd or Ni as catalyst) and HEAT → -C-C- with two H underneath

23
Q

condition and catalysts required for catalytic hydrogenation + what format are the catalysts in

A

heat and catalyst (Ni, Pt or Pd) –> finely divided or powdered form

24
Q

why are hydrogenation reactions not common in industry

A

as alkenes have higher demand then alkanes in industry

24
if no catalyst is used for hydrogenation, how can the reaction occur?
under strong heating
25
Conversion + equation of adding cold mno4 (aq) to alkene
Conversion of alkene to diol. C=C + [O] + H2O → -C-C- with 2 OH underneath
26
observation when cold acidified vs neutral vs alkaline MnO4 is added to alkene + reason
acidified: the solution changes from purple to colorless (oxidized from MnO4- to Mn2+) neutral and alkaline: the solution changes from brown to colorless as MnO2 is formed (manganese (IV) oxide is formed)
27
IF reaction occurs at a high temperature what will happen
side reactions may occur
28
why can acidified K2Cr2O7 not be used in the reaction
it is not strong enough to oxidize alkenes
29
definition of halogenation reaction
converts alkene to dihaloalkane
30
product when alkene react with cold acidified mno4
c-c with two hydroxyl groups underneath
31
observation when halogenation reaction occurs for alkene (+ provide reactant/condition)
react with X2 in organic solvent solution turns from (orange for bromine, yellow-green for chlorine, brown for iodine) to colorless
32
observation when halogenation reaction occurs for alkane (+ provide reactant/condition)
under light: solution turns from (orange for bromine, yellow-green for chlorine, brown for iodine) to colorless
33
is halogenation of alkene and alkane faster
alkene
34
state markovnikov's rule
markovnikov's rule states that when a molecule HX adds to a asymmetrical alkene, the hydrogen atom mainly attaches to the carbon atom that already carries the greater number of hydrogen atoms
35
when will only one haloalkane be formed in hydrohalogenation of alkene?
when the alkene is symmetrical
36