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TOPIC 6 - ORGANIC CHEM

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Test for purity of liquids

Back (Answer)

• Measure the boiling temp . More purity = closer to databook bp value. • Any impurities will raise the boiling temperature To determine bp: -substance heated above its bp, allowed to cool down and drawn into capillary tube and temp change.

#2
Front (Question)

extraction with a solvent in a separating funnel

Back (Answer)

• Add the chosen solvent to form 2 layers in a separating funnel (2 seperate liq with 2 diff densities) • Add stopper and gently shake • Allow the contents to settle into two layers • Remove the stopper and allow the lower layer to drain into a flask and the upper into a different flask

#3
Front (Question)

Drying with anhydrous salt

Back (Answer)

• Anhydrous calcium chloride to remove water and absorb moisture. • The drying agent (does not react with organic liq) can be removed by: • Filtration • Decanting

#4
Front (Question)

Simple Distillation

Back (Answer)

• separate liqs with very diff bp • easier to set up and quicker • only used if 25’C difference in bp 1. liq heated, liqs with low bp evaporates/boils off first and passes into condenser and collected in reciever seperately. Other liqs have higher bp evaporate off later. if temp begins to rise indicates diff compound boiling.

#5
Front (Question)

Fractional distillation

Back (Answer)

used to seperate liq. with similar bp - filled with glass beads/broken acts as an surface area which vapour leaving the column can condense. • Crude oil is heated in a furnace which turns most of it into vapour • Near the top is where the shorter chain molecules condense • Near the bottom is where longer molecules are as they have a higher melting point • Different columns have different temperatures where different length carbon chains condense

#6
Front (Question)

What is a hydrocarbon?

Back (Answer)

A compound that contains hydrogen and carbon only

#7
Front (Question)

What are saturated hydrocarbons?

Back (Answer)

Contain single bonds only. Hydrocarbons with the maximum amount of hydrogens possible

#8
Front (Question)

What are unsaturated hydrocarbons?

Back (Answer)

Contain 1 or more double bonds. Hydrocarbons without the maximum amount of hydrogens possible

#9
Front (Question)

empirical formula

Back (Answer)

The simplest whole number ratio of atoms in a compound

#10
Front (Question)

molecular formula

Back (Answer)

The actual number of atoms in each molecule

#11
Front (Question)

structural formula

Back (Answer)

Shows the arrangement of atoms carbon by carbon with the attached hydrogens and functional groups

#12
Front (Question)

skeletal formula

Back (Answer)

Shows the bonds of the carbon skeleton only, with any functional groups

#13
Front (Question)

displayed formula

Back (Answer)

Shows how all the atoms are arranged, and the bonds between them, drawn out

#14
Front (Question)

functional group

Back (Answer)

The group of atoms which gives an organic compound its characteristic properties and reactions

#15
Front (Question)

homologous series

Back (Answer)

A series of compounds with the same functional group and general formula and similar chemical properties, which differ by CH2 from the next member

#16
Front (Question)

general formula

Back (Answer)

alkenes - CnH2n alkanes - CnH2n+2 Haloalkane - CnH2n+1X Alcohols - CnH2n+1OH Aldehyde - CnH2n+1CHO Carboxylic acids - CnH2n+1COOH Ketone - CnH2nO carbonyl bond not at end of C chain when naming it has to be alphabetical and always count and write position of C in one direction.

#17
Front (Question)

addition react

Back (Answer)

Joining two or more molecules together to form a larger molecule

#18
Front (Question)

polymerisation

Back (Answer)

Joining together lots of simple molecules, same REPEATING UNITS - MONOMERS to form a large molecule - POLYMER.

#19
Front (Question)

Cis-trans isomerism / E-Z ISOMERISM

Back (Answer)

occur in alkenes Because the presence of C=C leads to restricted rotation, whereas in alkanes the atoms can rotate freely, without restriction. due to overlap of p-orbitals = pi bond. - TRIGONAL PLANAR 120’ - due to 3 areas of electron densities repel each other E = TRANS Z = CIZ - atoms/groups on each side with higher priority with higher Mr/Ar to determine E-Z isomerism • Ethene do not exhibit e/z as atoms are same on either side

#20
Front (Question)

crude oil

Back (Answer)

mainly made up of Alkanes. energy comes from burning fossil fuels, crude oil and natural gases. - Fractional distillation takes place: as chain length increases bp increases, volatility and viscosity, flammability and reactivity decreases.

#21
Front (Question)

3 main processes used to convert crude oil into fuels?

Back (Answer)

• Cracking • Reforming • Fractional distillation

#22
Front (Question)

Cracking

Back (Answer)

The breakdown of longer chain molecules into smaller ones by heating with a catalyst. Because the demand for longer chain hydrocarbons is much less than the demand for shorter chain hydrocarbons, therefore cracking is used to turn longer chain into shorter chain hydrocarbons • THERMALYTIC CRACKING - produces higher prop of alkanes and alkenes - 7000kPa - high temp 1200K • CATALYTIC CRACKING : - produces aromatic compounds/cyclic rings and H2 gas - low temps and normal press - zeolite catalyst

#23
Front (Question)

Reforming

Back (Answer)

conversion of straight chains alkanes/hydrocarbons into branched chain and cyclic hydrocarbons as they burn less efficiently when heated - so heated with a catalyst Pt helps it burn more smoothly in engine pentane = cyclopentane + H2 heptane = methylbenzene + 4H2

#24
Front (Question)

fractional distill

Back (Answer)

separate liq into fractions b boiling and condensing with similar bp near bottom, fractions with large moleculs and longer chains with high bp near top fractions with smaller molecules with low bp - rise higher up column and collected at the top. they condense and collect bottom fraction column = RPKDFB down the column fractions - incr in bp and decr in voltality and viscosity