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Organic 1st yr

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

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#1
Front (Question)

Functional group

Back (Answer)

is an atom or group of atoms which when present in different molecules causes them to have similar chemical properties

#2
Front (Question)

Homologous series

Back (Answer)

Homologous series are families of organic compounds with the same functional group and the same general formula. • They show a gradual change in physical properties (e.g. boiling point). • Each member differs by CH2 from the last. • same chemical properties

#3
Front (Question)

Order of priority highest first: CA, ALD, KET,halo, alke,alc

Back (Answer)

Carboxylic acids >aldehydes>ketones>alcohols>alkenes>halogenoalkanes

#4
Front (Question)

HOMOLYTIC FISSION

Back (Answer)

each atom gets one electron from the covalent bond When a bond breaks by homolytic fission it forms two Free Radicals. Free Radicals do not have a charge and are represented by a A Free Radical is a reactive species which possess an unpaired electron

#5
Front (Question)

HETEROLYTIC FISSION

Back (Answer)

one atom gets both electrons

#6
Front (Question)

Structural isomers

Back (Answer)

same molecular formula different structures (or structural formulae)

#7
Front (Question)

Chain isomers

Back (Answer)

Compounds with the same molecular formula but different structures of the carbon skeleton

#8
Front (Question)

position isomers

Back (Answer)

Compounds with the same molecular formula but different structures due to different positions of the same functional group on the same carbon skeleton

#9
Front (Question)

Functional group isomers

Back (Answer)

Compounds with the same molecular formula but with atoms arranged to give different functional groups

#10
Front (Question)

Stereoisomerism

Back (Answer)

Stereoisomers have the same structural formulae but have a different spatial arrangement of atoms

#11
Front (Question)

E-Z stereoisomers arise when: ab

Back (Answer)

(a) There is restricted rotation around the C=C double bond. (b) There are two different groups/atoms attached both ends of the double bond

#12
Front (Question)

Cahn–Ingold–Prelog (CIP) priority rules

Back (Answer)

• Compare the atomic number of the atoms directly attached to each side of the double bond; the atom of higher atomic number is given priority • If the atoms are the same, consider the atoms at distance 2 from the double bond. Make a list of each atom bonded to the one directly attached to the double bond. Arrange list in order of decreasing atomic number. Compare the lists atom by atom; at the earliest difference, the group containing the atom of higher atomic number is given priority

#13
Front (Question)

Priority Group:

Back (Answer)

The atom with the bigger atomic number is classed as the priority atom

#14
Front (Question)

Petroleum fraction

Back (Answer)

mixture of hydrocarbons with a similar chain length and boiling point range

#15
Front (Question)

Draw fractional destillation mechanism

Back (Answer)

Card back image
#16
Front (Question)

Key points to learn about fractional distillation

Back (Answer)

• Oil is pre-heated • then passed into the column. • The fractions condense at different heights • The temperature of the column decreases upwards • The separation depends on the boiling point. • Boiling point depends on the size of molecules. • The larger the molecule the larger the van der Waals forces • Similar molecules (size, bp, mass) condense together • Small molecules condense at the top at lower temperatures • and big molecules condense at the bottom at higher temperatures

#17
Front (Question)

Vacuum distillation unit

Back (Answer)

• Heavy residues from the fractionating column are distilled again under a vacuum. • Lowering the pressure over a liquid will lower its boiling point.

#18
Front (Question)

Fractional Distillation: In the laboratory

Back (Answer)

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#19
Front (Question)

Cracking:

Back (Answer)

conversion of large hydrocarbons to smaller hydrocarbon molecules by breakage of C-C bonds

#20
Front (Question)

Economic reasons for cracking

Back (Answer)

• The petroleum fractions with shorter C chains (e.g. petrol and naphtha) are in more demand than larger fractions. • To make use of excess larger hydrocarbons and to supply demand for shorter ones, longer hydrocarbons are cracked. • The products of cracking are more valuable than the starting materials (e.g. ethene used to make poly(ethene), branched alkanes for motor fuels, etc.

#21
Front (Question)

There are two main types of cracking:

Back (Answer)

thermal and catalytic

#22
Front (Question)

Thermal Cracking

Back (Answer)

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#23
Front (Question)

Catalytic Cracking

Back (Answer)

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#24
Front (Question)

Fuel :

Back (Answer)

releases heat energy when burnt