Back to marketplace

CD (from PMT Notes)

No description yet. This curated deck is ready for daily study.

Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What are dyes?

Back (Answer)

Coloured compounds that chemically bond to a substrate and absorb light in the visible spectrum.

#2
Front (Question)

What is a chromophore?

Back (Answer)

An atom or chemical group responsible for the colour of a compound.

#3
Front (Question)

Which functional groups can modify a chromophore?

Back (Answer)

• -OH • -NH2 • -NR2

#4
Front (Question)

How do dyes bond to fibers?

Back (Answer)

By intermolecular forces, covalent bonds, and ionic bonds.

#5
Front (Question)

What groups in fibers attract dyes?

Back (Answer)

• -COOH • -SO3H • -NH groups

#6
Front (Question)

What are auxochromes?

Back (Answer)

Functional groups that alter the solubility of a dye, such as carboxylic acid, sulfonic acid, amino, and hydroxyl groups.

#7
Front (Question)

What are triglyceride esters?

Back (Answer)

Esters formed from glycerol and carboxylic acids through esterification.

#8
Front (Question)

How does the chain length of carboxylic acids in triglycerides vary?

Back (Answer)

Ranges from C4 to C22.

#9
Front (Question)

Why do oils have a lower melting point than fats?

Back (Answer)

Oils are more unsaturated, containing more carbon-carbon double bonds.

#10
Front (Question)

What is the effect of carbon-carbon double bonds on oil molecules?

Back (Answer)

They alter the shape, preventing close packing and reducing melting point.

#11
Front (Question)

What are the main types of reactions?

Back (Answer)

• Addition • Substitution • Oxidation • Reduction • Hydrolysis • Condensation • Elimination

#12
Front (Question)

What defines an aromatic compound?

Back (Answer)

Compounds that contain a benzene ring.

#13
Front (Question)

What is the molecular formula of benzene?

Back (Answer)

C6H6.

#14
Front (Question)

What stabilizes benzene compared to other molecules?

Back (Answer)

The delocalised electron ring structure.

#15
Front (Question)

What is the enthalpy change of hydrogenation for benzene?

Back (Answer)

-208 kJ mol-1.

#16
Front (Question)

What does the bond length evidence from X-ray diffraction show about benzene?

Back (Answer)

All bond lengths between carbon atoms are the same.

#17
Front (Question)

Why does benzene not undergo electrophilic addition reactions?

Back (Answer)

It would break the stable delocalised ring of electrons.

#18
Front (Question)

What type of reaction does benzene undergo instead of electrophilic addition?

Back (Answer)

Electrophilic substitution reactions.

#19
Front (Question)

What is halogenation in relation to benzene?

Back (Answer)

A type of electrophilic substitution where benzene reacts with halogens in the presence of a catalyst.

#20
Front (Question)

What is nitration in the context of benzene?

Back (Answer)

An electrophilic substitution where NO2+ is the electrophile.

#21
Front (Question)

What is produced during the nitration of benzene?

Back (Answer)

Nitrobenzene

#22
Front (Question)

What does Friedel-Crafts acylation involve?

Back (Answer)

The nucleophilic attack of the benzene ring on acyl chlorides.

#23
Front (Question)

What are diazonium salts?

Back (Answer)

Salts containing the diazonium ion, R-N2+.

#24
Front (Question)

What happens when diazonium salts react with phenol?

Back (Answer)

They form azo compounds.