other organic chemistry Flashcards

1
Q

explain what is meant by fractional distillation

A

separation of compounds by their boiling points

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2
Q

nowadays used catalyst in cracking

what kind of catalyst is it

A

zeolite

heterogeneous catalyst

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3
Q

products of cracking are mostly

A

alkenes

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4
Q

understand octane rating

A

Hydrocarbons used in petrol (gasoline) are given an octane rating which relates to how effectively they perform in the engine. A hydrocarbon with a high octane rating burns more smoothly than one with a low octane rating.

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5
Q

octane rating is higher

A

in the isomers with branched chains. e.g. octane number of heptane is 0; octane number in 2,2,4-trimethylpentane is 100

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6
Q

isomerisation to increase octane rating condition

A

Pt catalyst on zeolite, 250 C, 13-30 atm

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7
Q

understand aromatic hydrocarbons

A

ones based on a benzene ring

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8
Q

how to improve the octane rating of hydrocarbons to be used in petrol

A
  1. isomerisation, or 2. reforming
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9
Q

conditions for reforming

A

a platinum catalyst suspended on aluminium oxide together with various promoters to make the catalyst more efficient. The original molecules are passed as vapours over the solid catalyst at a temperature of about 500°C.

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10
Q

what happens in reforming

A

Isomerisation reactions occur (as above) but, in addition, chain molecules get converted into rings with the loss of hydrogen.

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11
Q

reforming in hexane draw

A

hexane gets converted into benzene

http://www.chemguide.co.uk/physical/catalysis/petrochem.html

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12
Q

reforming in heptane draw

A

heptane gets converted into methylbenzene

http://www.chemguide.co.uk/physical/catalysis/petrochem.html

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13
Q

explain the use of crude oil as a source of both aliphatic and aromatic hydrocarbons

A

Crude oil is mainly a mixture of chains of carbon atoms. Some of these can be made into rings by a process called reforming, thus it is not only a source of aliphatic hydrocarbons but also of aromatic hydrocarbons

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14
Q

kmno4 solution acidified with dilute h2so4

A

purple solution becomes colorless

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15
Q

kmno4 solution made slightly alkaline (often by adding na2co3 solution)

A

the purple solution first becomes dark green solution, due to mno4 2- ions, and then produces a dark brown precipitate, due to solid mno2.

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16
Q

chem eq oxidation of ethene with cold dilute kmno4 solution

name of product

A

CH2=CH2 + H2O + [O] -> HOCH2CH2OH

ethane-1,2-diol

17
Q

full ioinic eq oxidation of ethene with cold dilute acidified kmno4 solution

A

5CH2=CH2 + 2H2O + 2MnO4- + 6H+ -> 5HOCH2CH2OH + 2Mn2+

18
Q

full ioinic eq oxidation of ethene with cold dilute alkaline kmno4 solution

A

At first: CH2=CH2 + 2MnO4- + 2OH- -> HOCH2CH2OH + 2MnO42-

But eventually: 3CH2=CH2 +2MnO4- + 4H2O -> 3HOCH2CH2OH + 2MnO2 + 2OH-

19
Q

full ionic eq oxidation of ethene with cold dilute kmno4 solution

A

neutral

3CH2=CH2 +2MnO4- + 4H2O -> 3HOCH2CH2OH + 2MnO2 + 2OH-

20
Q

CH3CH=C(CH3)2 with hot concentrated acidified kmno4 solution produce.. (word and chemical eq)

A

CH3COOH + CH3COCH3

ethanoic acid + propanone

21
Q

C4H8: but-1-ene, but-2-ene, 2-methylpropene differences in products with hot concentrated acidified kmno4 solution

A

CH2=CHCH2CH3 + 5[O] -> CO2 + H2O + CH3CH2COOH
CH3CH=CHCH3 + 2[O] -> 2CH3COOH
CH2C(CH3)2 + 4[O] -> CO2 + H2O + CH3COCH3

22
Q

describe and explain the inductive effects of alkyl groups on the stability of cations formed during
electrophilic addition

A

Alkyl groups tend to push electrons away, thus carrying a partial positive charge, and the carbon they are attached to carrying a partial negative charge. The alkyl group has a positive inductive effect.

if a charge is very localized the ion is much less stable than if the charge is spread out over several atoms.

From primary(least stable) to secondary to tertiary(most stable) carbocation, more alkyl groups present places more and more negative charge on the positive carbon, reducing charge density and stabilizing it.

23
Q

recognise the difficulty of the disposal of poly(alkene)s, i.e. nonbiodegradability and harmful combustion products

A

the disposal of poly(alkene) plastic waste is difficult, as much of it is chemically inert and non-biodegradable. When burnt, waste plastics may produce toxic products, such as hydrogen chloride from PVC (poly(chloroethene)), dioxins, and toxic CO from incomplete combustion of the hydrocarbons.

Separating other plastic waste from the poly(alkene)s when objects have just been thrown away without being sorted according to their recycle code is another difficulty recycling plants have.

24
Q

Solutions to the difficulty of the disposal of poly(alkene)s

A

burn the poly(alkene)s and use the energy released to generate electricity, help conserve our supplies of fossil fuels that currently generate most of our electricity.

Acidic gases would have to be neutralised before releasing the waste gas into the atmosphere and very high temperatures used in incinerators to break down any toxins.

25
Q

describe and explain how the combustion reactions of alkanes make them suitable to be used as fuels in industry, in the home and in transport

A

Alkanes are useful as fuels because they are readily available, convenient to transport and use, burn cleanly into co2 and h2o (as long as there is an excess of air or oxygen), and have high enthalpy changes of combustion.

26
Q

recognise the environmental consequences of unburnt hydrocarbons arising from the internal combustion engine

A

Small amounts of unreacted hydrocarbons from the petrol-air mixture are found in the exhaust fumes. Hydrocarbons in the atmosphere can absorb infra-red radiation and play a part in the greenhouse effect.

27
Q

three major commercial uses of esters

A

solvents, perfumes, flavourings

28
Q

outline the use of infra-red spectroscopy in monitoring air pollution

A

it identifies compounds, in this case, air pollutants, based on the change in vibrations of particular atoms when infra-red radiation of specific frequencies is absorbed

29
Q

note: pokoknya kalo alkene + cold dilute kmno4, acidified or alkaline gk peduli apa, pkoknya organic productnya itu taro -OH to all yg involved in double bonds di alkene reactantnya

A

uwaaaaahhh nicenice gotchotiiiii

30
Q

hcooh + fehling’s solution

A

positive result. red ppt.

31
Q

hcooh + tollen’s reagent

A

positive result. silver mirror.

32
Q

ch3cooh + fehling’s solution

A

negative result. solution remains blue.

33
Q

ch3cooh + tollens’ reagent

A

negative result. no visible reaction.

34
Q

in the carboxylic acids homologous series, only hcooh will give (+) result with fehling and tollen due to the resemblance of its structure with aldehyde

A

ooowowowo

35
Q

What have halogenated hydrocarbons been used for?

A

solvents, refrigerants, monomers in polymer manufacture