AQA A-Level Chemistry – Introduction to Organic Nomenclature

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13 flashcards summarizing key rules, priorities, examples, and common errors in IUPAC organic nomenclature.

Last updated 3:17 AM on 8/1/25
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13 Terms

1
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What is nomenclature in organic chemistry?

It is the system of naming organic compounds using standardized rules set by IUPAC.

2
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Why is IUPAC nomenclature important?

It gives every compound a unique, universally understood name, preventing confusion in scientific communication.

3
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What are the three main components of an IUPAC name?

Root (longest carbon chain), prefix (substituents/other functional groups), and suffix (main functional group).

4
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How is the root (stem) of an IUPAC name determined?

By counting the number of carbon atoms in the longest continuous chain that contains the highest-priority functional group.

5
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Give the standard root prefixes for 1–6 carbon atoms.

Meth (1), Eth (2), Prop (3), But (4), Pent (5), Hex (6).

6
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Name six common suffixes and the functional groups they represent.

–ane (alkanes), –ene (alkenes), –ol (alcohols), –al (aldehydes), –one (ketones), –oic acid (carboxylic acids).

7
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What is a position number in organic nomenclature?

A numeral indicating the carbon to which a functional group or substituent is attached, chosen to be as low as possible.

8
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State the main rules for naming branched alkanes.

1) Find the longest chain. 2) Identify and number alkyl substituents. 3) List substituents alphabetically with di-, tri-, etc. 4) Use numbers to show positions.

9
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When a molecule has multiple functional groups, how is one chosen for the suffix?

The group with the highest priority in the IUPAC hierarchy becomes the suffix; others are written as prefixes.

10
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Give the IUPAC priority order of these groups (highest to lowest): COOH, COOR, COCl, CHO, CO, OH, NH₂, C=C, C≡C, alkanes/halogens.

1 Carboxylic acids, 2 Esters, 3 Acid chlorides, 4 Aldehydes, 5 Ketones, 6 Alcohols, 7 Amines, 8 Alkenes, 9 Alkynes, 10 Alkanes/halogens.

11
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Using IUPAC rules, name CH₂=CHCH₂OH.

Prop-2-en-1-ol (alkene at C-2, alcohol given higher priority suffix).

12
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How are halogenoalkanes named? Give an example.

Use the prefixes fluoro-, chloro-, bromo-, or iodo- plus position numbers before the alkane name; e.g., CH₃CHClCH₃ is 2-chloropropane.

13
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List five common mistakes students make in organic nomenclature.

Incorrect chain numbering, ignoring longest chain, omitting position numbers, misusing prefixes/suffixes, not alphabetizing substituents.