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Module 4: Chapter 11&12 Organic Chemistry & Alkanes

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

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#1
Front (Question)

Define general formula

Back (Answer)

The simplest algebraic formula of a member of a homologous series e.g. CnH2n+2

#2
Front (Question)

Define structural formula

Back (Answer)

The minimal detail that shows the arrangement of atoms in a molecules e.g. CH3CH2CH2CH3

#3
Front (Question)

Define displayed formula

Back (Answer)

Shows the relative positioning of atoms and the bonds between them

#4
Front (Question)

Define skeletal formula

Back (Answer)

Simplified organic formula, shown by removing hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups

#5
Front (Question)

Define homologous series

Back (Answer)

A series of organic compounds having the same functional group but with each successive member differing by CH2

#6
Front (Question)

Define functional group

Back (Answer)

A group of atoms responsible for the characteristic reactions of a compound - alkanes is the only family that doesn’t have a functional group

#7
Front (Question)

Define aliphatic

Back (Answer)

A compound containing carbon and hydrogen joined together in straight chains, branched chains or non-aromatic rings

#8
Front (Question)

Define alicyclic

Back (Answer)

An aliphatic compound arranged in non-aromatic rings with or without side chains

#9
Front (Question)

Define aromatic

Back (Answer)

A compound containing a benzene ring

#10
Front (Question)

Define saturated

Back (Answer)

A molecule with single carbon to carbon bonds only

#11
Front (Question)

Define unsaturated

Back (Answer)

A molecule with multiple carbon-carbon bonds including double and triple carbon-carbon bonds and aromatic rings

#12
Front (Question)

Define structural isomers

Back (Answer)

compounds with the same molecular formula but with a different structural formulae

#13
Front (Question)

Define homolytic fissions

Back (Answer)

When a bond breaks and each bonding atom receives one electron from the bonded pair to form 2 radicals

#14
Front (Question)

Define heterolytic fission

Back (Answer)

When a bond breaks and one bonding atom receives both electrons from the bonded pair to form ions

#15
Front (Question)

Define radical

Back (Answer)

A species with an unpaired electron

#16
Front (Question)

What are the rules for naming alkanes?

Back (Answer)

• find the longest continuous carbon chain • identify any substituent group • number carbon atoms in longest chain to indicated position of any substituent groups (start numbering from the end that produces lowest set of numbers) • if same alkyl group appears more once indicated in name with di-, tri- and tetra- and use commas to separate numbers • names of different substituents are arranged alphabetically regardless of numbers

#17
Front (Question)

Why is carbon special?

Back (Answer)

• all carbon compounds are covalent • each carbon atom forms 4 covalent bonds • carbon forms strong covalent bonds with itself to form rings and chains

#18
Front (Question)

What are hydrocarbons?

Back (Answer)

only contain carbon and hydrogen and have the general formula CxHy

#19
Front (Question)

What is the molecular formula?

Back (Answer)

Gives the number of different types of atom in the molecule

#20
Front (Question)

What is the empirical formula?

Back (Answer)

Gives the ratio of the different types of atom in the molecule

#21
Front (Question)

What are the 3 types of structural isomers?

Back (Answer)

Chain, position and functional group

#22
Front (Question)

Describe position isomerism

Back (Answer)

in compounds containing a functional group, the functional group can be at different positions along the carbon chain

#23
Front (Question)

Describe functional group isomerism

Back (Answer)

molecules containing different functional groups have the same molecular formula

#24
Front (Question)

What are alkanes?

Back (Answer)

• hydrocarbons; they contain carbon and hydrogen only • they are saturated, only single carbon-carbon bonds • general formula of CnH2n+2