Biomolecules
Where Chemistry meets Biology. This chapter covers the chemical basis of life: Carbohydrates (Energy), Proteins (Structure/Enzymes), Vitamins (Regulators), and Nucleic Acids (Information). Focus on the Cyclic Structure of Glucose and Peptide bonds.
⚠️ Prerequisites
- Stereochemistry: D/L configuration (relative to Glyceraldehyde) vs d/l (optical rotation).
- Functional Groups: Reactions of Aldehydes (oxidation) and Alcohols (acetylation).
- Amides: Formation of amide bond (Peptide linkage).
🧠 Study Approach
Structure is Everything: Don't just read about Glucose; draw the Fischer projection and the Haworth projection. Understand why Glucose forms a hemiacetal ring (C1 attacks C5-OH).
🎯 How to Practice
Drawing Practice: Draw D-Glucose (Open chain), then cyclize it to $\alpha$-D-Glucopyranose. Memorize the positions of OH groups (Right-Left-Right-Right).
Linkage Logic: Differentiate linkages:
Peptide: $C-N$
Glycosidic: $C-O-C$
Phosphodiester: $P-O-C$.
Disease Table: Create a simple table: Vitamin | Name | Deficiency Disease. Memorize it. (e.g., Vit C - Ascorbic Acid - Scurvy).
📝 Quick Revision Notes
$NH_2OH$ $\to$ Oxime (Carbonyl group)
$Br_2/H_2O$ $\to$ Gluconic Acid (Aldehyde group)
$HNO_3$ $\to$ Saccharic Acid (Primary alcohol)
Pyrimidines: Cytosine (C), Thymine (T) (Uracil in RNA)
Pairing: A=T, G$\equiv$C
( dipolar ion, neutral overall )
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