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3.1 Introduction to Organic Chemistry

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Total cards: 11•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Empirical formula

Back (Answer)

Simplest whole number ratio of atoms in a molecule

#2
Front (Question)

Molecular formula

Back (Answer)

Gives the actual number of atoms of different elements 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 skeletal formula

Back (Answer)

Drawn as lines with each vertex being a carbon atom. Carbon atoms not drawn, assumed each C atom has all unspecified bonds as C-H

#6
Front (Question)

Define structural isomerism

Back (Answer)

When molecules have the same molecular formula but different structural formula

#7
Front (Question)

What is positional isomerism?

Back (Answer)

Functional group is attached to the main chain at a different place

#8
Front (Question)

What is functional group isomerism?

Back (Answer)

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

#9
Front (Question)

What is chain isomerism?

Back (Answer)

Hydrocarbon chain organised differently e.g. branched chains

#10
Front (Question)

Define stereoisomerism.

Back (Answer)

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

#11
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 (zusammen) isomer If they are on different sides, it is the E (entgegen) isomer