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P2 7 Organic chem (crude oil)

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Total cards: 21•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (21)

#1
Front (Question)

describe how crude oil forms

Back (Answer)

• fossil fuel formed over millions of years • biomass (mainly dead plankton) falls to sea bed, covered in layers of mud • mud turns into rock and dead organisms decay forming oil

#2
Front (Question)

describe the composition of crude oil

Back (Answer)

• a mixture of many different compounds • mostly hydrocarbons- most found in crude oil are alkanes

#3
Front (Question)

state the formula for alkanes

Back (Answer)

C(n) H(2n+2)

#4
Front (Question)

state the first four alkanes

Back (Answer)

CH4 methane C2H6 ethane C3H8 propane C4H10 butane

#5
Front (Question)

describe the process of fractional distillation of crude oil

Back (Answer)

• crude oil vaporised (heated) so most alkane molecules turn into a gas • gas put in the bottom of a fractionating column where it is hottest • (as it is gas) they rise up the column and start to cool, once an alkane reaches its boiling point it condenses into a liquid and is collected -> crude oil molecules with extremely high boiling points will not vaporise, so are collected at the bottom of the column as a thick/sticky liquid -> long-chain hydrocarbons have higher boiling points so condense quicker+ will be collected near the bottom of the column

#6
Front (Question)

describe the temperature gradient of a fractionating column

Back (Answer)

gets cooler as you move up the column (oil begins as a gas and condenses as a liquid)

#7
Front (Question)

describe the fractions produced from crude oil by fractional distillation (from long to short chain hydrocarbons / bottom to top of column)

Back (Answer)

• bitumen (unvaporised molecules remain as liquid, thick/sticky mixture) - tar for roads/roofs • fuel oil - ships • diesel oil - trucks/lorries • kerosene - plane fuel • petrol - cars • LPG (gas- doesn’t condense) - liquified for fuel or burned for domestic heating/cooking (methane/ethane..)

#8
Front (Question)

define volatility+ volatile

Back (Answer)

volatility- how easily a liquid vaporises volatile- a chemical that vaporises easily (so also easily flammable)

#9
Front (Question)

describe the boiling point of short vs long chain hydrocarbons

Back (Answer)

short - low as they are volatile (collected at top of column) long - high (collected at bottom of column)

#10
Front (Question)

describe the flammability of short vs long chain hydrocarbons

Back (Answer)

short - high (as they are volatile) long - low

#11
Front (Question)

define viscosity and viscous

Back (Answer)

viscosity - how easily a liquid flows (how thick it is) viscous - a chemical that doesn’t flow easily, gloopy/thick

#12
Front (Question)

describe the viscosity of short vs long chain hydrocarbons

Back (Answer)

short - low, runny long - high (viscous), thick

#13
Front (Question)

state the equation for the complete combustion of hydrocarbons

Back (Answer)

CnH2n+2 + O2 -> CO2 + H2O hydrocarbon + oxygen -> carbon dioxide + water

#14
Front (Question)

describe the main use of hydrocarbons

Back (Answer)

• used for fuels • shorter-chain hydrocarbon molecules are best as they are more flammable so require less energy • hydrocarbons are oxidised during combustion -> produces carbon dioxide + water + ENERGY released

#15
Front (Question)

state the equation for the incomplete combustion of hydrocarbons

Back (Answer)

hydrocarbon + oxygen -> carbon monoxide OR carbon (soot) + water

#16
Front (Question)

describe why cracking is used on hydrocarbons

Back (Answer)

• long-chain hydrocarbons are broken down into smaller-chain molecules -> smaller molecules are more useful for fuels as they are more flammable • also produces alkenes which are used to make polymers (plastic)

#17
Front (Question)

state the equation for cracking

Back (Answer)

long-chain alkane -> shorter-chain alkane + alkene

#18
Front (Question)

are alkenes more/less reactive than alkanes

Back (Answer)

(also hydrocarbons) more reactive than alkanes as they contain a double carbon bond (C=C) -> used to make polymers (plastics)

#19
Front (Question)

describe the test for alkenes

Back (Answer)

bromine water changes from orange-brown to colourless for a positive result -> alkanes don’t react with bromine water

#20
Front (Question)

describe catalytic cracking (4)

Back (Answer)

• used to crack long-chain alkanes • produces moderate-chain alkanes used for fuels • requires a lower temperature • uses a catalyst (silica, SiO2) in powder form, increases SA to speed up the breakdown

#21
Front (Question)

describe steam cracking (3)

Back (Answer)

• used to crack moderate-chain alkanes • produces short-chain alkanes used for petrochemicals • requires a higher temperature • also produces alkenes used for polymers (plastics)