A camping stove uses propane (C₃H₈).
If 44 g of propane is completely burned:
C3H8+5O2→3CO2+4H2O
How many grams of CO₂ are produced?
132 g CO₂
Electrophilic substitution in pyrrole occurs mainly at which position — 2 or 3? Why?
Position 2 (α-position)
More resonance stabilization of sigma complex.
Why Does Onion Make You Cry?
Onions release sulfur-containing compounds (e.g., sulfoxides).
When cut, they form a volatile compound that reacts with water in your eyes to produce a mild acid → irritation and tears.
I’m made of ethene, long and strong, I last forever — don’t come along! Which polymer chain am I in the throng?
Polyethylene
Why does acetylene (C₂H₂) produce a hotter flame than methane (CH₄)?
Acetylene has a triple bond (higher energy).
It releases more energy during combustion → hotter flame (~3300°C)
Which is most sensitive to acidic conditions: pyrrole, furan, or thiophene?
Furan (least aromatic stability).
Why Is Paracetamol Less Acidic Than Aspirin?
Aspirin contains a carboxylic acid (-COOH) group → strongly acidic.
Paracetamol contains a phenol (-OH) group → weaker acid.
Carboxylic acids are more acidic because their conjugate base is more resonance stabilized.
I dissolve polish in a flash, My carbonyl group does the dash. Which solvent am I in your stash?
Acetone (ketone –C=O)
Why doesn’t benzene undergo addition reactions easily like alkenes?
Because benzene is aromatic and very stable (Hückel rule: 4n+2 π electrons).
Addition would destroy aromatic stability.
Suggest a method to synthesize pyrrole from a 1,4-dicarbonyl compound.
Paal–Knorr synthesis
Why Is Soap Able to Remove Oil?
Soap molecules have:
Long nonpolar hydrocarbon tail
Polar carboxylate head
They form micelles, trapping oil inside.
Interaction involved: Hydrophobic interaction.
I fight radicals, keep cells free,
I donate electrons, that is me.
Which vitamin am I, can you see?
Vitamin C (ascorbic acid)
In darkness I am silent and slow, But under UV light I start to glow. Chlorine splits — radicals appear, They attack methane without fear. Initiation, propagation, termination too, Chain reaction — I continue through. Who am I?
Reaction: Chlorination of methane
Mechanism: Free radical substitution
Initiation step: Cl₂ → 2Cl• (homolytic cleavage)
Which 5-membered heterocycle is present in:
Vitamin B1 (Thiamine)?
Tiazol
Why Does Cooking Meat Produce Aroma?
Amino groups (proteins)
Carbonyl groups (sugars)
This produces complex aromatic organic compounds responsible for flavor.
C–F bonds make me tough,
Nothing sticks — that’s enough.
Which polymer surface is this stuff?
Teflon (PTFE)
You nitrate toluene using HNO₃/H₂SO₄.
❓ Tasks:
Predict major products.
Explain directing effect.(Mechanism)
1. ortho-nitrotoluene
para-nitrotoluene
2. Electrophilic aromatic substitution
Which 5 membered heterocyle is available in Korrin Porfin va Billuribin?
Pyrrole
Why Does DNA Contain Nitrogen Heterocycles?
Nitrogen heterocycles (purines & pyrimidines):
Are aromatic → stable
Form hydrogen bonds
Enable specific base pairing
Aromaticity contributes to structural stability of DNA.
I’m in syrups and candies too,
I taste like sugar, but I’m not you.
Which polyol keeps desserts sweet through?
Glycerol (–OH groups / sugar alcohol)