JEE Main & Advanced

Chemistry in Everyday Life

Chemistry in Everyday Life for JEE Main & Advanced

1
Module 1

Drugs and Their Action

Classification of Drugs and Drug-Receptor InteractionTopic 1

Drugs: Chemicals of low MW ($\sim 100$ to $\sim 500$ Da) that interact with biological targets to produce a therapeutic response. Used to treat, cure, or prevent disease.

Pharmacology: Study of drugs and their effects on living systems.

Chemotherapy: Use of chemicals to treat disease, especially infections and cancer.

Classification of Drugs:

A. Based on Pharmacological Effect:

ClassFunctionExamples
AnalgesicsReduce painAspirin, paracetamol, morphine
AntipyreticsReduce feverAspirin, paracetamol
Anti-inflammatoryReduce inflammationIbuprofen, naproxen
AntisepticsKill microbes on living tissueDettol, iodine tincture
DisinfectantsKill microbes on non-living surfacesChlorine, phenol, bleaching powder
AntibioticsKill bacteriaPenicillin, chloramphenicol, ampicillin
AntihistaminesTreat allergiesDiphenhydramine, cetirizine
AntacidsNeutralize stomach acid$Al(OH)_3$, $Mg(OH)_2$
TranquilizersReduce anxiety, sedateDiazepam (Valium), barbiturates
AntifertilityBirth controlNorethindrone, estrogen

B. Based on Drug Action:

  • Agonist: Mimics natural messenger; binds receptor and activates it. (e.g., morphine mimics endorphins)
  • Antagonist: Blocks receptor; doesn't activate. (e.g., naloxone blocks morphine receptors)

C. Based on Chemical Structure:

  • Sulfa drugs, $\beta$-lactams, etc.

D. Based on Molecular Target:

  • Enzyme inhibitors (e.g., aspirin inhibits cyclooxygenase, COX)
  • Receptor binders (e.g., morphine binds opioid receptors)

Drug-Receptor Interaction:

Receptors: Proteins (mostly membrane proteins) that recognize specific chemical messengers (hormones, neurotransmitters).

Mechanism:

  1. Drug binds to receptor site (often by hydrogen bonds, ionic, dipole, van der Waals).
  2. Conformational change in receptor → signal transduction.
  3. Cellular response (e.g., neurotransmitter release, enzyme activation).

Enzyme Inhibitors:

  • Competitive: Drug structure resembles substrate; competes for active site (e.g., methotrexate competes with folate).
  • Non-competitive: Binds elsewhere; changes enzyme shape (allosteric).
  • Irreversible: Binds covalently; permanently inactivates enzyme (e.g., penicillin binds enzyme that makes bacterial cell wall).

Drug Design Strategy:

  • Identify target (enzyme, receptor).
  • Design drug to fit binding site precisely.
  • Modify to enhance specificity, reduce side effects.
Worked Examples
1

Classify the following drugs by function: aspirin, dettol, ibuprofen, penicillin, antacid, diazepam.

Show solution
  • Aspirin: Analgesic + antipyretic + anti-inflammatory.
  • Dettol: Antiseptic.
  • Ibuprofen: Anti-inflammatory + analgesic.
  • Penicillin: Antibiotic.
  • Antacid (e.g., $Mg(OH)_2$): Neutralizes acid in stomach.
  • Diazepam: Tranquilizer (anxiety reduction).

Final Answer: Each has specific function as listed.

2

Explain how a competitive inhibitor works.

Show solution

A competitive inhibitor is a molecule that:

  1. Has a structure similar to the natural substrate of an enzyme.
  2. Binds to the active site of the enzyme.
  3. Competes with substrate for the active site.
  4. Doesn't undergo the chemical reaction (or reacts very slowly).

Result: Reduces enzyme activity; the rate of normal reaction decreases.

Example: Methotrexate competes with folic acid for the enzyme dihydrofolate reductase. Used in cancer therapy (cancer cells need rapid folate metabolism).

By increasing substrate concentration, the effect of competitive inhibitor can be overcome (more substrate competes back successfully).

Final Answer: Mimics substrate; competes at active site; reversible.

✎ Self-Check — 5 questions0 / 5
Q1.

Antacids treat:

Q2.

Penicillin is:

Q3.

Aspirin is also a/an:

Q4.

Drug-receptor binding is by:

Q5.

Competitive inhibitor:

Antimicrobials, Antiseptics, AntibioticsTopic 2

Antimicrobials: Substances that kill or inhibit microorganisms (bacteria, viruses, fungi, protozoa).

Categories:

1. Antiseptics:

  • Applied to living tissue (skin, wounds).
  • Examples: Dettol (mix of chloroxylenol + terpineol), tincture of iodine ($2-3\%\,I_2$ in alcohol/water), savlon, $H_2O_2$, KMnO₄ (mild), boric acid (eye wash).
  • Furacin, soframycin (creams).

2. Disinfectants:

  • Applied to non-living surfaces (floors, instruments).
  • Examples: chlorine ($Cl_2$ in water), phenol ($1\%$ — antiseptic; concentrated — disinfectant), formaldehyde, hypochlorous acid (bleach), sulfur dioxide, bleaching powder.

Note: Same substance can be antiseptic or disinfectant depending on concentration:

  • $0.2\%$ phenol: antiseptic
  • $1\%$ phenol: disinfectant

3. Antibiotics:

Definition: Substances produced (in nature) by microorganisms that kill or inhibit growth of other microorganisms. Now also synthesized.

Classification by Spectrum:

  • Broad spectrum: Effective against many types of bacteria (gram-positive and gram-negative). e.g., ampicillin, tetracycline, chloramphenicol.
  • Narrow spectrum: Effective against only specific types. e.g., penicillin G (against gram-positive only).

Classification by Action:

  • Bactericidal: Kill bacteria. e.g., penicillin, aminoglycosides.
  • Bacteriostatic: Inhibit bacterial growth (let immune system clear infection). e.g., chloramphenicol, tetracycline, erythromycin.

Common Antibiotics:

AntibioticTypeDiscoveryAction
Penicillin$\beta$-lactamA. Fleming (1928)Inhibits bacterial cell wall synthesis
StreptomycinAminoglycosideWaksman (1943)Inhibits protein synthesis
TetracyclineTetracyclineDuggar (1948)Inhibits 30S ribosome
ChloramphenicolSynthetic (originally from Streptomyces)1947Inhibits 50S ribosome
ErythromycinMacrolide1952Inhibits 50S ribosome
Ampicillin/Amoxicillin$\beta$-lactam, semi-syntheticModified penicillinCell wall
CiprofloxacinFluoroquinoloneSyntheticInhibits DNA gyrase

Antibiotic Resistance: Repeated/improper use of antibiotics causes bacteria to evolve resistance (mutations, transfer of resistance genes via plasmids). Major public health issue.

4. Sulfa Drugs (Sulfonamides):

  • Synthetic antibacterial drugs (pre-penicillin era).
  • Sulfanilamide ($H_2N-C_6H_4-SO_2NH_2$) → many derivatives.
  • Mechanism: Competitive inhibition of bacterial enzyme dihydropteroate synthase (mimics PABA — para-aminobenzoic acid).

5. Antifungal: Nystatin, ketoconazole, fluconazole. 6. Antiviral: Acyclovir, AZT (against HIV).

Common Analgesics:

DrugTypeMechanism
Aspirin ($C_6H_4(OCOCH_3)COOH$, acetylsalicylic acid)NSAIDInhibits COX enzyme (reduces prostaglandins)
Paracetamol (Acetaminophen, $C_6H_4(OH)NHCOCH_3$)Non-opioidInhibits COX in CNS (no anti-inflammatory)
IbuprofenNSAIDCOX inhibitor
NaproxenNSAIDCOX inhibitor
MorphineOpioid (narcotic)Binds μ-opioid receptors in brain

Aspirin Properties:

  • Acetylsalicylic acid
  • Reduces fever, pain, inflammation
  • Anti-platelet: prevents blood clotting → used for heart attack prevention
  • Side effects: stomach ulcers, Reye's syndrome (in children)

Antacids:

Excess HCl in stomach → acidity, ulcers.

Common antacids:

  • $Mg(OH)_2$ (milk of magnesia)
  • $Al(OH)_3$
  • $NaHCO_3$ (sodium bicarbonate, "soda")
  • $CaCO_3$
  • Modern: Ranitidine (Zantac), omeprazole (Prilosec) — inhibit histamine-2 receptors or proton pump (more targeted)

Antihistamines:

Histamine causes allergic reactions (runny nose, itching, hives).

Examples: Brompheniramine (Dimetapp), terfenadine (Seldane), cetirizine, loratadine, diphenhydramine. Mechanism: Block $H_1$ receptors.

Worked Examples
1

Distinguish antiseptic and disinfectant.

Show solution
PropertyAntisepticDisinfectant
Applied toLiving tissue (skin, wounds)Non-living surfaces (floors, instruments)
ToxicityLow (safe for skin)Higher
ExamplesDettol, tincture iodine, savlonChlorine, phenol (conc.), formaldehyde
Concentration of phenol$0.2\%$$1\%$

Final Answer: Antiseptics for skin; disinfectants for non-living surfaces.

2

What is the mechanism of penicillin's antibacterial action?

Show solution

Penicillin contains a $\beta$-lactam ring (4-membered N-containing cyclic amide). It mimics the structure of bacterial cell-wall components.

Mechanism:

  1. Penicillin binds covalently to the active site of transpeptidase (enzyme that cross-links peptidoglycan in bacterial cell walls).
  2. The strained $\beta$-lactam ring is highly reactive; it acylates the enzyme's serine residue.
  3. Transpeptidase is irreversibly inhibited.
  4. Bacteria cannot complete cell wall synthesis → cell wall weak → bacteria lyse.

Penicillin is specific to bacteria because human cells don't have peptidoglycan walls.

Final Answer: Irreversibly inhibits bacterial transpeptidase via $\beta$-lactam ring opening → no cell wall → lysis.

✎ Self-Check — 5 questions0 / 5
Q1.

Dettol is a/an:

Q2.

Aspirin's chemical name:

Q3.

Antibiotic that inhibits cell wall synthesis:

Q4.

Broad spectrum antibiotic:

Q5.

Antacids treat:

2
Module 2

Cleansing Agents and Food Chemistry

Soaps, Detergents, and Surface ActivityTopic 1

Cleansing Agents: Substances that remove dirt and grease from surfaces by emulsifying them in water.

Two main types: soaps and synthetic detergents (syndets).

1. Soaps:

Definition: Sodium or potassium salts of long-chain fatty acids ($C_{12}$ to $C_{18}$).

Common examples:

  • Sodium stearate: $CH_3(CH_2)_{16}COONa$
  • Sodium palmitate: $CH_3(CH_2)_{14}COONa$
  • Sodium oleate: $CH_3(CH_2)_7CH=CH(CH_2)_7COONa$ (unsaturated)

Manufacture (Saponification): $$\text{Fat/Oil (triglyceride)} + 3NaOH \to \text{Soap} + \text{Glycerol}$$

Triglyceride = triester of glycerol with three fatty acids. $$CH_2(OOCR)-CH(OOCR')-CH_2(OOCR'') + 3NaOH \to RCOONa + R'COONa + R''COONa + CH_2(OH)CH(OH)CH_2OH$$

Types of Soaps:

  • Hard soap (sodium soap): From animal fat with NaOH. Soft, slightly soluble.
  • Soft soap (potassium soap): From vegetable oils with KOH. Liquid, more soluble.
  • Toilet soap: From high-quality fats; less alkali; with perfume.
  • Medicated soap: Contains antiseptic.
  • Transparent soap: Dissolved in alcohol.
  • Shaving soap: Contains glycerol (prevents drying); stearic acid.

Cleansing Action of Soap:

Soap is a surfactant — has two parts:

  • Hydrophilic head: $-COO^-Na^+$ (water-loving)
  • Hydrophobic tail: Long alkyl chain (oil-loving)

In water above critical micelle concentration (CMC):

  • Tails huddle together (avoid water); heads project outward.
  • Form spherical aggregates: micelles.
  • Heads on outside (in water); tails inside (in dirt/grease).

For washing:

  1. Soap reduces surface tension of water.
  2. Tails dissolve in grease/dirt; heads in water.
  3. Micelles form around dirt, suspending it.
  4. Rinsing washes micelles (with dirt inside) away.

Limitations of Soaps:

  • Hard water: Contains Ca²⁺, Mg²⁺. These form insoluble Ca/Mg salts of fatty acids (scum):

$2C_{17}H_{35}COONa + Ca^{2+} \to (C_{17}H_{35}COO)_2Ca \downarrow + 2Na^+$

  • Wastes soap; leaves residue on clothes.
  • Doesn't work in acidic water (fatty acid precipitates out).

2. Synthetic Detergents (Syndets):

Designed to overcome hard water limitations.

Classification:

TypeStructureExampleProperty
Anionic-ve charged headSodium dodecylbenzene sulfonate ($R$-$C_6H_4$-$SO_3^-Na^+$)Laundry, household cleaners
Cationic+ve charged headCetyltrimethylammonium bromide ($CH_3(CH_2)_{15}N^+(CH_3)_3 Br^-$)Hair conditioners, fabric softeners; germicidal
Non-ionicNo charge; uses ether/-OH groupsPolyethylene glycol stearateLiquid detergents, sensitive skin

Sodium Dodecylbenzene Sulfonate (SDBS): $CH_3-(CH_2)_{11}-C_6H_4-SO_3^-Na^+$

Advantages over soap:

  • Works in hard water (Ca/Mg salts of sulfonate are soluble — no scum)
  • Works in acidic water
  • Stronger cleansing
  • Can be tailored for specific uses

Biodegradability:

  • Straight chain: Biodegradable; broken down by microbes.
  • Branched chain: Not biodegradable; persists in water; environmental pollution.
  • Modern detergents are linear (linear alkyl benzenesulfonates, LAS) for environmental reasons.
Worked Examples
1

Why does soap not work well in hard water?

Show solution

Hard water contains dissolved Ca²⁺ and Mg²⁺ ions (from CaCO₃, MgCO₃, sulfates).

When soap (e.g., sodium stearate, $C_{17}H_{35}COONa$) is added: $2C_{17}H_{35}COONa + Ca^{2+} \to (C_{17}H_{35}COO)_2Ca \downarrow + 2Na^+$ $2C_{17}H_{35}COONa + Mg^{2+} \to (C_{17}H_{35}COO)_2Mg \downarrow + 2Na^+$

The calcium and magnesium salts of fatty acids are insoluble — they form scum (white floating residue). Until all Ca²⁺/Mg²⁺ removed, soap doesn't form lather; it's wasted.

This is why synthetic detergents (with sulfonate group) are preferred: Ca and Mg sulfonate salts ARE soluble → no scum.

Final Answer: Hard water Ca²⁺/Mg²⁺ form insoluble scum with soap; detergents don't have this issue.

2

Explain cleansing action of soap with diagram.

Show solution

Soap molecule = hydrophobic tail + hydrophilic head.

Step 1: In water, soap molecules orient: tails away from water, heads in water. Excess form micelles (~$50-100$ molecules; spherical with tails inside).

Step 2: When dirty cloth (with grease/oil) immersed:

  • Hydrophobic tails of micelles enter the grease/oil
  • Heads project outward into water

Step 3: Mechanical action (rubbing) detaches grease from cloth.

Step 4: Detached grease is trapped inside micelle (oil droplet now surrounded by soap layer with heads outward).

Step 5: Rinsing washes these grease-filled micelles away → cleaned cloth.

Final Answer: Dual nature of soap forms micelles around oil → emulsion → rinsed away.

✎ Self-Check — 5 questions0 / 5
Q1.

Soap is:

Q2.

Saponification gives:

Q3.

Hard water + soap:

Q4.

Anionic detergent example:

Q5.

Cationic detergent is used in:

Food Additives, Preservatives, Artificial SweetenersTopic 2

Food Additives: Substances added to food to:

  • Preserve (prevent spoilage)
  • Enhance flavor, color, texture
  • Replace nutrients

Types:

1. Preservatives: Prevent spoilage caused by microorganisms.

PreservativeUse
Sodium benzoate ($C_6H_5COONa$)Soft drinks, jams, jellies, juices
Sodium metabisulfite ($Na_2S_2O_5$)Wine, fruit juices, dried fruits
Sodium nitrate / nitriteCured meats (bacon, ham) — prevents botulism
Salt (NaCl)Traditional; preserves meat, fish
SugarJams, preserves; high osmotic pressure
Vinegar (acetic acid)Pickles
Propionate saltsBread (prevents mold)
Sorbic acid / potassium sorbateCheese, wine, baked goods

2. Antioxidants:

Prevent oxidation (rancidity) of fats/oils.

AntioxidantUse
BHA (Butylated Hydroxyanisole)Cereals, fats, baked goods
BHT (Butylated Hydroxytoluene)Similar to BHA
Vitamin E (tocopherol)Natural antioxidant; oils, supplements
Vitamin C (ascorbic acid)Beverages, fruit products
Sulfur dioxide ($SO_2$)Wine, dried fruits
TBHQFrying oils

Mechanism: They donate hydrogen atom to free radicals; preferentially oxidized themselves, sparing the food.

3. Artificial Sweeteners:

Provide sweetness with little or no calories. Important for diabetics and weight management.

SweetenerBrand nameRelative sweetness (vs sucrose)Notes
SaccharinSweet'N Low$\sim 500\times$Earliest (1879); some carcinogenic concerns (now reduced)
AspartameNutraSweet, Equal$\sim 100\times$Made from aspartic acid + phenylalanine; warnings for phenylketonurics (PKU)
SucraloseSplenda$\sim 600\times$Made by chlorinating sucrose; heat-stable
Stevia (steviol glycosides)Truvia, Stevia$\sim 300\times$Natural (from Stevia plant)
Alitame$\sim 2000\times$Made from aspartic + alanine amide
Acesulfame-KSunett$\sim 200\times$Heat-stable; used in baking
Cyclamate$\sim 30\times$Banned in US; used elsewhere

4. Food Colors:

  • Natural: beta-carotene (orange), chlorophyll (green), curcumin (yellow), anthocyanin (purple/red).
  • Synthetic: tartrazine (yellow), sunset yellow, erythrosine (red), brilliant blue.

5. Flavor Enhancers:

  • Monosodium glutamate (MSG): umami flavor; debated health effects.
  • 5'-nucleotides (GMP, IMP): synergize with MSG.

6. Emulsifiers/Stabilizers/Thickeners:

  • Lecithin, mono-/diglycerides, gums (guar, xanthan, locust bean).
  • Carrageenan, agar (from seaweed).
  • Pectin, starches.

7. Anti-caking Agents:

  • Silicon dioxide, calcium silicate, magnesium stearate.
  • Prevent powders (salt, sugar) from clumping.

Spoilage of Food (How preservatives work):

Microbial spoilage: Bacteria, yeast, mold grow on food. Preservatives create unfavorable conditions:

  • pH (acetic acid, lactic acid)
  • Osmotic pressure (high salt/sugar)
  • Direct toxicity (sulfites, benzoates)

Oxidative spoilage: Fats and oils undergo oxidation → rancidity. Antioxidants prevent.

Enzymatic spoilage: Natural enzymes in food cause browning (fruit cut). Antioxidants (Vitamin C) prevent.

Worked Examples
1

Compare aspartame and saccharin.

Show solution
PropertySaccharinAspartame
Sweetness vs sucrose~$500$×~$100$×
StructureCyclic imide of $o$-sulfobenzoic acidDipeptide of aspartic acid + phenylalanine methyl ester
Heat stabilityStableDecomposes when heated; not for baking
CalorieZeroVery low (peptide-based)
ConcernsEarlier carcinogen concern (largely refuted)Avoid in phenylketonuria (PKU); breaks down to methanol

Final Answer: Different structures and stability; aspartame is dipeptide-based (avoid in PKU).

2

Why is sodium benzoate used as preservative in soft drinks?

Show solution

Sodium benzoate ($C_6H_5COONa$) is the sodium salt of benzoic acid.

Mechanism:

  1. In acidic conditions (soft drinks are acidic), sodium benzoate → benzoic acid (un-ionized).
  2. Un-ionized benzoic acid can cross microbial cell membranes.
  3. Inside the cell, it dissociates (cytoplasm is neutral) → benzoate anion.
  4. This disrupts microbial pH and enzymes → inhibits growth.

Effective against yeasts, molds, and some bacteria — common spoilage organisms.

Sodium benzoate is safe at low concentrations (recommended < $1$ g/kg food).

Final Answer: Inhibits microbial growth by acidifying cell interior; safe at low doses.

✎ Self-Check — 5 questions0 / 5
Q1.

Common preservative in soft drinks:

Q2.

Aspartame is:

Q3.

Most sweet (relative to sucrose):

Q4.

Antioxidant in food:

Q5.

MSG enhances:

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