PYQ Vault

MHT-CET Chemistry · Teaching notes

Biomolecules — MHT-CET Chemistry

Biomolecules is about two questions a paper in MHT-CET Chemistry and almost never HARD — two of its past-year questions in eighty-eight. It is a chapter of named facts with a small amount of counting: which sugar is which and what its ring is, the reactions that prove glucose's structure, the glycosidic linkage in every disaccharide and polysaccharide, the twenty amino acids by class and code, protein shape, and the numbering of the purine and pyrimidine bases, the sugar and the phosphate in a nucleotide. Five pages in the book's order. Every PYQ is tagged.

Every subtopic, worked example, formula and trap in one printable document — answers shown, ready to share.

Subtopic notes

PYQ weightage by concept

9 concepts · 88 PYQs — where the marks actually sit, so you know what to drill first

Carbohydrates: Classification, Structure and Reactions21 PYQs · 24%
ConceptPYQsShare
Classification, and the Structures of Glucose and Fructose1416%
Reactions of Glucose: What Each One Proves78%
Glycosidic Linkages in Di- and Polysaccharides19 PYQs · 22%
ConceptPYQsShare
Sucrose, Maltose, Lactose, Raffinose, Stachyose: the Linkage and the Hydrolysis Count1315%
Starch, Glycogen and Cellulose67%
Amino Acids, Peptides and Proteins27 PYQs · 31%
ConceptPYQsShare
The Amino Acids by Side Chain: Class, Code and the Essential Ones1719%
Peptide Bonds, Protein Shape and Structure Levels1011%
Nucleic Acids: Nucleotides, Bases and the Double Helix16 PYQs · 18%
ConceptPYQsShare
Nucleotide Anatomy: Sugar, Base and Phosphate by Position1416%
The Phosphodiester Backbone and the Watson–Crick Double Helix22%
Lipids, Enzymes and Other Biomolecules5 PYQs · 6%
ConceptPYQsShare
Triglycerides, Fatty Acids, Soap and Enzymes56%

Formula & revision sheet

7 formulas · 2 reference tables · 9 gotchas across all subtopics — the exam-eve cheat-sheet

Carbohydrates: Classification, Structure and Reactions

Formulas (2)

  • Classification, and the Structures of Glucose and Fructose · Glucose and fructose rings
    Glucose: C-1 (CHO)+C-5 OH→pyranose (hemiacetal);Fructose: C-2 (C=O)+C-5 OH→furanose (hemiketal)\text{Glucose: C-1 (CHO)} + \text{C-5 OH} \to \text{pyranose (hemiacetal)};\quad \text{Fructose: C-2 (C=O)} + \text{C-5 OH} \to \text{furanose (hemiketal)}
  • Reactions of Glucose: What Each One Proves · Mild and strong oxidation
    Glucose→Br2/H2Ogluconic acid (1 COOH);Glucose→conc. HNO3saccharic acid (2 COOH)\text{Glucose} \xrightarrow{\text{Br}_2/\text{H}_2\text{O}} \text{gluconic acid (1 COOH)};\quad \text{Glucose} \xrightarrow{\text{conc. HNO}_3} \text{saccharic acid (2 COOH)}

Watch out for (2)

Glycosidic Linkages in Di- and Polysaccharides

Formulas (1)

  • Starch, Glycogen and Cellulose · Three glucose polymers
    amylose: α-1,4;amylopectin / glycogen: α-1,4+α-1,6;cellulose: β-1,4\text{amylose: } \alpha\text{-1,4};\quad \text{amylopectin / glycogen: } \alpha\text{-1,4} + \alpha\text{-1,6};\quad \text{cellulose: } \beta\text{-1,4}

Reference tables (1)

Sucrose, Maltose, Lactose, Raffinose, Stachyose: the Linkage and the Hydrolysis Count5 rows
SugarUnitsLinkageReducing?Glucose per mole
MaltoseGlucose + glucosealpha-1,4Yes2
LactoseGalactose + glucosebeta-1,4Yes1
SucroseGlucose + fructoseC-1 (alpha-Glc) to C-2 (beta-Fru)No1
Both anomeric carbons are in the bond — hence non-reducing and invert sugar on hydrolysis.
RaffinoseGal + Glc + FruTrisaccharideNo1
Stachyose2 Gal + Glc + FruTetrasaccharideNo1
Maltose is the only common disaccharide that gives two glucose per mole.
Amino Acids, Peptides and Proteins

Formulas (1)

Reference tables (1)

The Amino Acids by Side Chain: Class, Code and the Essential Ones12 rows
Amino acid3-letter / 1-letterSide chain RClass
GlycineGly / G–HNeutral, achiral
AlanineAla / A–CH₃Neutral
SerineSer / S–CH₂OHNeutral
ThreonineThr / T–CH(OH)CH₃Neutral, essential
MethionineMet / M–CH₂CH₂SCH₃Neutral, essential, has S
Leucine / ValineLeu / L · Val / Visobutyl · isopropylNeutral, essential
TryptophanTrp / WindolylmethylNeutral, essential, heterocyclic
Aspartic acidAsp / D–CH₂COOHAcidic
D is aspartic acid; E is glutamic acid.
Glutamic acidGlu / E–CH₂CH₂COOHAcidic
LysineLys / K–(CH₂)₄NH₂Basic, essential
ArginineArg / RguanidinoBasic
HistidineHis / HimidazolylmethylBasic, essential, heterocyclic
The one that is basic, essential and heterocyclic at once — the favourite answer.
Class follows the side chain: a second COOH is acidic, a second basic N is basic, everything else neutral.
Nucleic Acids: Nucleotides, Bases and the Double Helix

Formulas (2)

Lipids, Enzymes and Other Biomolecules

Formulas (1)

  • Triglycerides, Fatty Acids, Soap and Enzymes · Triglyceride hydrolysis
    triglyceride+3 H2O→glycerol+3 RCOOH;linolenic acid: C18, 3 C=C\text{triglyceride} + 3\,\text{H}_2\text{O} \to \text{glycerol} + 3\,\text{RCOOH};\qquad \text{linolenic acid: } \text{C}_{18},\ 3\ \text{C=C}

Watch out for (1)