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Organic 1 Section 3 - Unit 11: Introduction to Organic Chemistry

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Total cards: 19•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (19)

#1
Front (Question)

Define empirical formula

Back (Answer)

Simplest whole number ratio of atoms in a molecule

#2
Front (Question)

Define molecular formula

Back (Answer)

Actual ratio of the number of atoms in a molecule

#3
Front (Question)

Define displayed formula

Back (Answer)

Shows every atom and every bond in a molecule

#4
Front (Question)

Define structural formula

Back (Answer)

Shows arrangement of atoms in a molecule without showing every bond

#5
Front (Question)

Define structural isomer

Back (Answer)

Compounds with the same molecular formula but different structural formula

#6
Front (Question)

Define positional isomer

Back (Answer)

Compounds where the functional group is attached to the main chain at a different place

#7
Front (Question)

What is functional group isomerism

Back (Answer)

Same atoms but a different functional group due to a different arrangement of atoms

#8
Front (Question)

What is chain isomerism

Back (Answer)

Hydrocarbon chain is organised differently

#9
Front (Question)

Define stereoisomerism

Back (Answer)

When molecules have the same structural and molecular formula, but have a different arrangement of atoms in space

#10
Front (Question)

What is E-Z isomerism and how are the E and Z isomers decided?

Back (Answer)

• E-Z isomerism is caused by the limited rotation about C=C double bonds • If the two substituents with the highest molecular mass are on the same side of the double bond, it is the Z isomer • If they are on different sides, it is the E isomer

#11
Front (Question)

State two general features of an homologous series of compounds (2 marks)

Back (Answer)

• Same functional group - Same general formula

#12
Front (Question)

How is the unpaired electron in a radical represented?

Back (Answer)

By a dot before or after the molecule

#13
Front (Question)

Define homolytic fission

Back (Answer)

• The breakage of a bond to form 2 free radicals - Each atom gets one electron from the covalent bond

#14
Front (Question)

Define free radical

Back (Answer)

A reactive species which possess an unpaired electron

#15
Front (Question)

Define heterolytic fission

Back (Answer)

• The breakage of a bond to form ions - One atom gets both electrons from the covalent bond

#16
Front (Question)

How is the formation of a covalent bond shown?

Back (Answer)

By a curly arrow that starts from a lone electron pair or from another covalent bond

#17
Front (Question)

How is the breakage of a covalent bond shown?

Back (Answer)

By a curly arrow starting from the bond

#18
Front (Question)

When do E-Z stereoisomers form? (2)

Back (Answer)

• When there is restricted rotation around the C=C double bond. • When there are two different groups attached both ends of the double bond

#19
Front (Question)

Explain the CIP rules used to determine the name of an alkene

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