Veda Bites are swipeable micro-lessons — each one teaches exactly one
idea. The bites below come from this kit — swipe through them in the app.
💡 Key Idea
Alkanes Are Saturated — That's Their Whole Identity
Single bonds only. No exceptions.
Alkanes are saturated hydrocarbons — they contain only carbon-carbon single bonds and C-H bonds, with no double or triple bonds anywhere.
↳ If a molecule has any double or triple bond, it is NOT an alkane.
📖 Definition
Why Alkanes Are Called 'Paraffins'
Latin for 'little affinity' — and it fits.
Alkanes are highly inert toward common reagents like $KMnO_4$, sodium dichromate, nitric acid, and hydrogen peroxide. This lack of reactivity earned them the name paraffins.
↳ Alkane inertness is a direct consequence of strong, stable sigma bonds.
💡 Key Idea
sp³ Hybridization Builds the Tetrahedral Frame
Every carbon sits at a tetrahedron's center.
In alkanes, each carbon is sp³ hybridized, giving a tetrahedral geometry with bond angles of about $109.5^\circ$.
↳ sp³ hybridization explains both the shape and the stability of alkanes.
➗ Formula
The General Formula for Alkanes
One formula, every alkane.
This formula defines the homologous series of alkanes — same functional behavior, different chain lengths.
↳ Plug in n to get the molecular formula of any alkane.
💡 Key Idea
Root Words: Name Follows Carbon Count
Count carbons, pick the root.
↳ The root word is fixed by the number of carbons in the parent chain.
💡 Key Idea
Primary Suffixes Reveal the Bond Type
One suffix tells you the bond.
For alkanes, the primary suffix is always -ane.
↳ Root + primary suffix = IUPAC name of the alkane.
⚙️ Process
Naming a Branched Alkane: Step-by-Step
Longest chain first. Always.
↳ Longest chain → lowest locants → alphabetical order. That's the IUPAC sequence.
✏️ Example
Worked Example: 2,3,5-Trimethylhexane
Left gives 11. Right gives 11. Now what?
An 8-carbon chain with methyl groups at positions 2, 3, 5, 6 from the left gives sum = 16; from the right gives 11. So numbering starts from the right.
↳ Lowest sum of locants decides the numbering direction.
⚠️ Common Mistake
Don't Number From the Wrong End
Lowest first substituent beats lowest sum? Not always.
↳ One substituent → lowest single locant. Multiple → lowest sum.
⚖️ Comparison
Straight-Chain vs Branched Alkanes
Same formula, different boiling points.
↳ Branching reduces surface contact → weaker intermolecular forces → lower boiling point.
⭐ Important Fact
Physical State Follows Chain Length
Gas → liquid → solid as carbons grow.
↳ All alkanes are colorless and odorless — only the physical state changes with size.
⭐ Important Fact
Solubility: Nonpolar Means Water-Shy
Like dissolves like — alkanes avoid water.
Alkanes are nonpolar, so they do not dissolve in polar solvents like water but dissolve readily in nonpolar solvents such as benzene, ether, and carbon tetrachloride.
↳ Nonpolar nature explains both insolubility in water and solubility in organic solvents.
⭐ Important Fact
Boiling Point Climbs ~20–30 °C Per CH₂
Add one CH₂, raise the boil by 20–30 °C.
↳ Boiling point is regular; melting point is not — don't confuse the two trends.
❓ Did You Know
Even-Carbon Alkanes Melt Higher
Even carbons pack better — and melt higher.
Alkanes with an even number of carbon atoms have higher melting points than their odd-numbered neighbors because they pack more symmetrically, allowing greater intermolecular attraction.
↳ Even-carbon alkanes pack better → higher melting point.
🎯 Exam Tip
Exam Favorite: Why Are Alkanes Inert?
This question appears every year.
↳ Three keywords — sp³, sigma bonds, nonpolar — earn full marks.