JEE Chemistry Hydrocarbons
Hydrocarbons PDF Notes, Important Questions and Synopsis
SYNOPSIS
- Alkanes: General formula: CnH2n+2
- Preparation of alkanes
- Chemical properties of alkanes
- Aromatisation:
- Cracking (pyrolysis):
Conformations →
Eclipsed
Staggered
Skew
Conformation in
which hydrogen atoms attached to two carbon atoms are as close to each other as possible
Conformation in which hydrogen atoms are as farther away as possible
Any other intermediate
conformation in between eclipsed and sawhorse
Sawhorse projection
Newman projection
- Preparation of alkanes
- Geometrical isomers of alkenes
Trans-isomer is non-polar and has zero dipole moment where a cis-isomer is polar.
Cis-isomer has higher boiling points compared to trans-isomer because it is polar.
In case of solids, cis-isomer has a lower melting point than trans-isomer. This is because the trans-isomer is symmetrical and fits well into the crystal lattice.
. Preparation of alkenes
Chemical properties of alkenes
Test for Unsaturation: There are two tests to know whether a compound is unsaturated or not
- Bromine water test: When an unsaturated compound is reacted with bromine solution in carbon tetrachloride, the reddish-orange colour of bromine solution in carbon tetrachloride is discharged.
- Baeyer’s reagent test: When an unsaturated compound is reacted with cold, dilute and aqueous solution of potassium permanganate (Baeyer’s reagent), the pink colour of KMnO4 solution is discharged.
- Bromine water test: When an unsaturated compound is reacted with bromine solution in carbon tetrachloride, the reddish-orange colour of bromine solution in carbon tetrachloride is discharged.
- Preparation of alkynes
Acidic nature of alkynes: Hydrogen atoms of ethyne attached to triple bonded carbon atom are acidic in nature.
Example:Reason:
Alkyne
Alkene
Alkane
Hybridisation of carbon to which H atom is attached
sp
sp2
sp3
Percentage s character of carbon
50%
(maximum)
66.6%
25%
(minimum)
Electronegativity of carbon atom
Highest
Less than alkyne and more than alkane
Lowest
Extent of attraction of hydrogen atoms of C-H bonds towards C
Highest
Less than alkyne and more than alkane
Lowest
Ease of liberation of H atoms as protons
Highest
Less than alkyne and more than alkane
Lowest
Acidic character
Highest
Less than alkyne and more than alkane
Lowest
Chemical properties of alkynes
- Benzene:
Conditions for aromaticity
- Planarity: The ring should be planar. In simple words, all the carbons of the ring should be sp2 hybridised.
- Complete delocalisation of the p electrons in the ring: The p electrons should be completely delocalized. In simple words, in the ring alternate single and double bonds should exist.
- Hückel Rule: Presence of (4n + 2) p electrons in the ring where n is an integer (n = 0, 1, 2, . . .).

- Ortho–para directing groups: Groups which direct the incoming group to
ortho and para positions are called ortho–para directing groups.
Activating groups: Groups which increase the electron density at ortho and para positions of the benzene ring.
Examples: –NH2, –NHR, –NHCOCH3, –OCH3, –CH3 and –C2H5.Deactivating groups: Groups which decrease the electron
density at ortho and para positions of the benzene ring.
Example: –X. - Meta directing groups: The groups which direct the incoming group to meta position are called meta directing groups.
Examples: –NO2, –CN, –CHO, –COR, –COOH, –COOR and –SO3H.
Videos
JEE Class Revise
- PH of solution that is 0.1M NaA and 0.1M HA(Ka=1×10^-6) would be
- Please solve both 1&2 assertion and reason type questions with detailed explanation.
ThanQ!
- This isomerisation reaction is possible
through
a resonance
b enolization
c generation of carbanion
d generation of carbocation
- what happened when p nitro ethylbenzene is treated with bromine in presence of fe
- I could find only 4 structural isomers, but the answer provided is 5. Please help me find the fifth isomer.
- Why is option (a) said to be the most stable and not option (b) ?
- What is the order of Electrophilic Aromatic Substitution reactions?
- Should we give more priority to the rule that resonance structure with all atoms having octet is more stable ,or, to the rule that more electronegative atom should have negative charge on it and less electronegative atom should have positive charge on it, while deciding between stability of resonance structures? What will be the answer of the questions a and b in the picture then?
Kindly Sign up for a personalised experience
- Ask Study Doubts
- Sample Papers
- Past Year Papers
- Textbook Solutions
Sign Up
Verify mobile number
Enter the OTP sent to your number
Change