CBSE · Class 12 · Chemistry · Chapter 10
Biomolecules — Formula Sheet
- 1.Molecular Formula of Glucose
Open-chain form has 5 –OH groups and one –CHO. Cyclic (pyranose) form is 6-membered ring — α and β anomers differ at C-1.
- 2.Sucrose Hydrolysis (Inversion of Sugar)★
Sucrose is dextrorotatory but the product mixture is levorotatory (fructose has larger −ve rotation) — hence 'invert sugar'.
- 3.Reducing vs Non-reducing Sugars★
Reducing sugars have a FREE hemiacetal/hemiketal (open-chain aldehyde/ketone available). Detected by Tollens', Fehling's, Benedict's test.
- 4.Peptide Bond Formation★
Condensation of –COOH of one amino acid with –NH₂ of next. The C–N amide bond is planar and partially double-bond (resonance).
- 5.Zwitterion (Amino Acid at Isoelectric Point)
At isoelectric pH the amino acid exists as a dipolar ion. Solid amino acids have high m.p. and are crystalline because of ionic zwitterion form.
- 6.Chargaff's Rules (Base Pairing in DNA)★
Purines (A, G) pair with pyrimidines (T, C). Two H-bonds in A=T pair, three in G≡C pair.
- 7.α-Amino Acid General Structure
20 standard α-amino acids in proteins. Except glycine (R = H), all α-carbons are chiral ⇒ optically active. All natural amino acids are L-series (S-configuration except cysteine).
- 8.Michaelis-Menten Equation
: Reaction velocity · : Maximum velocity (at saturating [S]) · : Substrate concentration · : Michaelis constant
Basic enzyme kinetics. Km = [S] at which v = v_max/2; small Km ⇒ high affinity.
- 9.Glycosidic Linkage Classification
α-linkage: digestible by humans (starch, glycogen). β-linkage: indigestible fibre (cellulose).