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Aliphatic Compounds Reviewer

The document provides a comprehensive overview of aliphatic compounds, including their structure, naming conventions, and functional groups. Key points include the importance of numbering carbon chains, identifying branches, and understanding the impact of branching on hydrogen counts. It also covers IUPAC naming rules and examples of complex compound names, emphasizing the significance of functional groups in determining reactivity.

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0% found this document useful (0 votes)
86 views4 pages

Aliphatic Compounds Reviewer

The document provides a comprehensive overview of aliphatic compounds, including their structure, naming conventions, and functional groups. Key points include the importance of numbering carbon chains, identifying branches, and understanding the impact of branching on hydrogen counts. It also covers IUPAC naming rules and examples of complex compound names, emphasizing the significance of functional groups in determining reactivity.

Uploaded by

erichchloe2311
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOCX, PDF, TXT or read online on Scribd

🔬 CONSUMER CHEMISTRY REVIEWER: ALIPHATIC COMPOUNDS +

FUNCTIONAL GROUPS

🧠 60-SECOND SUMMARY: 5 Key Points About Aliphatic Compounds


1. Carbon Chain Numbering
o Always find the longest straight chain (parent chain).
o Start numbering from the end closest to a branch or
functional group.
o Goal: Give the lowest possible number to any side chain or
reactive group.
2. Branches (Substituents)
o –CH3 is methyl, –CH2CH3 is ethyl, –CH2CH2CH3 is propyl, –
CH2CH2CH2CH3 is butyl.
o Put the carbon number before the branch: 2-methylbutane
(CH3 on carbon 2).
o Use di-, tri-, tetra- if there’s more than one of the same group:
 Ex: 2,3-dimethylpentane (methyl groups on carbons 2 and
3)
3. Hydrogen Adjustment in Branching
o Carbon makes 4 bonds. If you add a branch, remove a
hydrogen.
o A carbon with a methyl branch becomes –CH2– (not –CH3).
4. Structure Types
o Expanded: Shows all atoms and bonds.
o Condensed: Groups atoms (CH3CH2CH3).
o Line: Each point is a carbon; hydrogens are not shown, but
assumed.
5. IUPAC Naming Rules
o Find the longest chain → number it → name the branches and
their positions → add suffix (-ane, -ene, -yne).
o Example: 3-ethyl-2-methylpentane

🧪 DETAILED LESSON RECAP


🔹 What Are Aliphatic Compounds?
 Chains that can be straight or branched (but not rings like benzene).
 Types:
o Alkanes: Single bonds only
o Alkenes: At least one double bond
o Alkynes: At least one triple bond

🔗 Functional Groups + Aliphatic Compounds


 Functional group = part of the molecule that reacts.
 Common examples:
o –OH = alcohol (ends in -ol)
o –COOH = carboxylic acid (-oic acid)
o C=C = alkene (-ene)
o C≡C = alkyne (-yne)
o –CHO = aldehyde (-al)
o –CO– = ketone (-one)

🧾 Naming Complex Compounds (Examples + Logic)


1. hept-2-yne
 Hept = 7 carbon chain
 -yne = triple bond
 2 = triple bond starts at carbon 2
 Why not 2-heptyne? Because “2-heptyne” can sound like the branch is
on carbon 2 — hept-2-yne is clearer.
2. 3-methylpent-1-yne
 5 carbon chain (pent), triple bond on C1
 Methyl branch on C3
3. 2,3-dimethylbutane
 Butane = 4 carbons
 Methyl groups on C2 and C3
 Use di- since it’s two of the same group
4. 3-ethyl-2-methylpentane
 7 carbon chain
 Ethyl (–CH2CH3) on C3
 Methyl (–CH3) on C2
 Alphabetical order in naming: ethyl before methyl
5. pent-2-en-4-yne
 5 carbon chain
 Double bond on C2, triple bond on C4
 Both are included in name using en-yne system
🧬 Why Does Hydrogen Decrease in Branching?
 Carbon needs 4 bonds.
 If a branch replaces a hydrogen, one hydrogen is lost.
 Ex: CH3 becomes CH2 when a branch is added.

🧩 Functional Group Questions You Might Be Asked


1. What is a functional group?
o A group of atoms that changes how the molecule reacts.
2. Give an example of a compound with a functional group and a
branch.
o Example: 3-methylbutan-1-ol (alcohol + methyl branch)
3. Functional group vs branch?
o Functional group = reactive part (like –OH)
o Branch = extra carbon chain (like –CH3)
4. How do you find the parent chain?
o Choose the longest chain that includes the functional group or
multiple bond.
5. What is an isomer?
o Same formula, different structure.
6. di-, tri-, tetra- meanings?
o 2, 3, and 4 of the same branch or group.
7. How do alkanes, alkenes, and alkynes differ?
o Alkanes = single bonds
o Alkenes = double bonds
o Alkynes = triple bonds
8. Examples of physical property questions
o Flammability of alkanes? → Yes, hydrocarbons burn easily.
o Reactivity? → Alkenes and alkynes are more reactive than
alkanes.
9. What are line structures?
o Each point = carbon atom.
o Branches = small lines off the chain.
o Functional groups shown using symbols (–OH, =O, etc.)
10. If there are multiple functional groups?
 Follow priority order: Carboxylic acid > Aldehyde > Ketone > Alcohol
> Alkene > Alkyne
🧪 More Challenging Names You Might See
 3,3-dimethylhex-1-yne → 6 carbons, triple bond at C1, 2 methyl
groups on C3
 4-ethyl-2-methylheptane → 7 carbon chain, ethyl on C4, methyl on
C2
 pent-2-en-4-yne → double bond on C2, triple bond on C4

🧠 Final Tips
 Always number the chain to give the lowest number to the main
group.
 Know suffixes and priorities.
 Always double-check bond counts.
 Practice naming and drawing often!

“If you can name it, you can draw it. If you can draw it, you
understand it.”
We got this. 💯

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