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HYDROGEN
▢ Basic Facts:
- •Discoverer → Henry Cavendish
- •Old name → inflammable air
- •1st element in periodic table
- •Atomic mass → 1.008 amu
- •Electronegativity → 2.1
- •Name coined by Lavoisier → hydrogen = water former
- •Occurrence → free state + combined state
- •Earth crust → nearly 1% by weight
- •Position in periodic table → debatable
- •Also called → rogue element
▢ Position in Periodic Table:
- •Resembles alkali metals
- •Resembles halogens
- •Usually placed at top left of periodic table above group IA
- •Kept separated from alkali metals due to distinctive characters
▢ Resemblance with Alkali Metals:
- •Electronic configuration → 1s¹
- •One outermost electron like alkali metals → ns¹
- •Cation formation → H(1s¹) → H⁺ + e⁻
- •H⁺ = smallest cation
- •Combines with halogens → halides
- •Combines with oxygen → oxides
- •Combines with sulphur → sulphides
- •Displaced from acids by metals → electropositive character
- •Acts as reducing agent like alkali metals
▢ Reducing Examples:
- CuO + H₂ → Cu + H₂O
- B₂O₃ + 6K → 2B + 3K₂O
▢ Resemblance with Halogens:
- •Diatomic gas like F₂ and Cl₂
- •One electron short of stable configuration
- •Forms hydrides with alkali and alkaline earth metals, similar to halides
- •Ionization enthalpy closer to halogens than alkali metals
▢ Hydride and Halide Analogy:
- H₂ + 2Na → 2NaH
- Cl₂ + 2Na → 2NaCl
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PREPARATION OF HYDROGEN
▢ By Action of Water on Active Metals:
❖ Principle: Metals above hydrogen in electrochemical series liberate H₂ from water/acids.
❖ Reactions:
- 2Na + 2H₂O → 2NaOH + H₂↑
- Zn + H₂SO₄ → ZnSO₄ + H₂↑
❖ Notes:
- •Higher position above H in electrochemical series → more vigorous reaction
- •Zn + dilute H₂SO₄ = laboratory method
- •Pure Zn not used because reaction is slow
- •Concentrated H₂SO₄ not used because SO₂ is evolved instead of H₂
- •Metals like Mg and Mn give small amount of H₂ with very dilute HNO₃
- •H₂ bubbles may stick to Zn surface and stop further reaction
- •Small amount of CuSO₄ prevents this by activating Zn surface
▢ By Action of Alkali on Amphoteric Metals:
❖ Metals: Zn, Al, Pb, Sn, As, Sb
❖ Reactions:
- Zn + 2NaOH → Na₂ZnO₂ + H₂↑
- 2Al + 2NaOH + 2H₂O → 2NaAlO₂ + 3H₂↑
❖ Products:
- Na₂ZnO₂ → sodium zincate
- NaAlO₂ → sodium aluminate
❖ Special: Al + NaOH method = Uyeno's process
▢ By Action of Water on Metal Hydrides:
- LiH + H₂O → LiOH + H₂↑
- CaH₂ + 2H₂O → Ca(OH)₂ + 2H₂↑
▢ Hydrolith:
- •CaH₂ = hydrolith
- •Formation: Ca + H₂ → CaH₂
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INDUSTRIAL PREPARATION OF HYDROGEN
▢ Electrolysis of Water:
- •Water contains small amount of acid/alkali: 15–20%
- •H₂ liberated at cathode, usually iron cathode
- •O₂ liberated at anode, usually nickel-plated iron rod
- •Anode and cathode separated by asbestos diaphragm
- •Asbestos diaphragm prevents mixing of H₂ and O₂
- •Very pure H₂ obtained by electrolysis of Ba(OH)₂ solution because it is carbonate-free
▢ Water Gas / Bosch Process:
❖ Step 1: Water Gas Formation: C + H₂O → CO + H₂
❖ Condition: Red hot coke + steam, 440–600°C
❖ Step 2: Water Gas Shift: CO + H₂ + H₂O → CO₂ + 2H₂
❖ Catalyst: Fe₂O₃
❖ Promoter: Cr₂O₃
❖ Temperature: 440–550°C
❖ Purification: CO₂ removed by washing gaseous mixture with water under pressure
❖ Nature: Redox process
▢ Lane's Process: 3Fe + 4H₂O → Fe₃O₄ + 4H₂
▢ From Natural Gas:
❖ Reaction: CH₄ + H₂O → CO + 3H₂
❖ Catalyst: Ni or Cr
❖ Temperature: 900°C
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PHYSICAL PROPERTIES OF HYDROGEN
▢ General:
- •Tasteless gas
- •Odourless gas
- •Colourless gas
- •Lightest element
- •Lightest gas
▢ Occlusion:
❖ Meaning: Adsorption/absorption of H₂ by metals.
❖ Metals: Fe, Au, Pt, Pd, Ni
❖ Occluded Hydrogen:
- •Hydrogen adsorbed by metals
- •Purest form of hydrogen
- •Used for purification of hydrogen
- •Released when metal is heated in vacuum
❖ Order: Colloidal Pd > crystalline Pd > Pt > Au > Ni > Fe
❖ Special: Powdered Pd can occlude nearly 1000 times its own volume of H₂.
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CHEMICAL PROPERTIES OF HYDROGEN
▢ Combustion:
- •Combustible gas
- •Burns in air/O₂ with nearly invisible pale blue flame
▢ Reducing Property:
- •Reduces heated metallic oxides to metals
- •Elements above hydrogen in electrochemical series are not reduced by H₂
- •Examples not reduced by H₂ → Zn, Al, alkali metal oxides, alkaline earth metal oxides
▢ Reduction Reaction: CuO + H₂ → Cu + H₂O
▢ Hydrogenation:
- •Converts unsaturated compounds to saturated compounds
- •Catalyst → Ni
▢ Hydrogenation Reactions:
- CH₂=CH₂ + H₂ → CH₃–CH₃
- Vegetable oil + H₂ → vegetable ghee / vanaspati ghee
▢ Hardening of Vegetable Oil:
❖ Catalyst: Finely divided Ni
❖ Condition: High pressure, about 400°C
❖ Product: Solid fat / vanaspati ghee
▢ Uses in Flame:
- •Liquid H₂ → cryogenic fluid
- •Oxy-hydrogen flame → cutting and welding steel
- •Atomic hydrogen flame → cutting and welding hard metals
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DIFFERENT FORMS OF HYDROGEN
▢ Atomic Hydrogen:
- •Obtained by passing ordinary hydrogen through electric arc at about 2000°C
- •Formation is endothermic
- •Absorbed heat is stored in atoms
- •Also prepared by irradiating hydrogen with mercury radiation
- •Highly unstable
- •Half-life about 0.3 second
- •Atoms combine readily to form H₂ with large heat liberation
- •Does not combine with nitrogen
- •Can be isolated
- •Cannot be prepared at room temperature
- •Strongest reducing form of hydrogen
▢ Atomic Hydrogen Reductions:
- BaSO₄ + 8H → BaS + 4H₂O
- CO₂ + 2H → HCOOH
- CO + 2H → HCHO
- P₂O₅ → PH₃
▢ Nascent Hydrogen:
- •Freshly produced hydrogen in contact with substance to be reduced
- •Also called newborn hydrogen
- •Cannot be isolated
- •More active than ordinary molecular hydrogen
- •Generated in situ
▢ Nascent Hydrogen Examples:
- Zn + H₂SO₄ → ZnSO₄ + 2H
- Fe³⁺ + H → Fe²⁺ + H⁺
- Acidified KMnO₄: purple → colourless
▢ Nascent Hydrogen Note:
- •Ordinary H₂ does not reduce acidified KMnO₄ or FeCl₃ directly
- •Nascent H produced in the same solution reduces them
- •Nascent H cannot be isolated, but atomic H can be isolated
▢ Active Hydrogen:
- •Obtained by silent electric discharge through molecular hydrogen
- •Temperature: 60–80°C
- •Exists at periphery of sun
- •Used in hydrogen welding
- •Hydrogen torch used in hydrogen welding
▢ Reducing Power Order: Ordinary H₂ < Nascent H < Active H < Atomic H
▢ Ortho and Para Hydrogen:
❖ Nature: Nuclear spin isomers of hydrogen.
❖ Ortho Hydrogen:
- •Spins of two protons in same direction
- •More stable than para form
- •Ordinary hydrogen at 25°C contains 75% ortho form
❖ Para Hydrogen:
- •Spins of two protons in opposite directions
- •Lower energy form
- •Favoured at low temperature
- •At absolute zero, only para form exists
❖ Important Ratios:
- At 25°C equilibrium mixture → ortho : para = 3 : 1
- At 35 K → ortho : para = 1 : 1
- Lower temperature → para percentage increases
- Above 800°C → ortho percentage increases
❖ Other Points:
- Para hydrogen tends to revert into ortho hydrogen
- Thermal conductivity: para-H₂ > ortho-H₂
- Atomic H converts para-H₂ into ortho-H₂
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ISOTOPES OF HYDROGEN
Table 1: Isotopes of hydrogen
Isotope | Symbol | Proton | Electron | Neutron | Remarks |
|---|---|---|---|---|---|
Protium | ¹H₁ / H | 1 | 1 | 0 | Most abundant |
Deuterium | ²H₁ / D | 1 | 1 | 1 | Heavy hydrogen; forms heavy water |
Tritium | ³H₁ / T | 1 | 1 | 2 | Radioactive |
▢ Important Points:
- •Protium forms simple water
- •Deuterium forms heavy water
- •Tritium is radioactive
- •Ordinary hydrogen: protium : deuterium = 6400 : 1
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USES OF HYDROGEN
▢ Liquid Hydrogen:
- •Rocket fuel
- •High calorific value
- •High heating ratio
- •Small mass
- •Large quantity of heat production
- •Cryogenic fluid to maintain low temperature
▢ Hydrogen Economy:
❖ Meaning: Use of liquid hydrogen as alternate energy source.
❖ Advantages:
- •More energy per unit weight of fuel
- •No pollution by CO, SO₂, hydrocarbons, lead etc.
- •High efficiency: 70–85%
- •Fuel cells convert H₂–O₂ chemical energy into electrical energy
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HYDRIDES
▢ Definition: Compounds formed by combination of hydrogen with metals or non-metals.
▢ Types:
- Ionic / salt-like / saline hydrides
- Molecular / covalent hydrides
- Metallic / interstitial hydrides
- Polymeric hydrides
- Complex hydrides
▢ Ionic / Salt-like / Saline Hydrides:
- •Hydrogen oxidation state → −1
- •Formed by highly electropositive metals
- •Formed mainly by alkali and alkaline earth metals except Be and Mg
- •Example: CaH₂ / hydrolith
- •Crystalline solids
- •Conduct electricity in fused state
- •Used as solid fuel
▢ Thermal Stability of Ionic Hydrides:
- LiH > NaH > KH > RbH > CsH
- CaH₂ > SrH₂ > BaH₂
▢ Molecular / Covalent Hydrides:
- •Hydrogen oxidation state → +1
- •Formed by highly electronegative elements / non-metals
- •Mostly covalent
- •Molecules held by weak van der Waals forces
▢ Stability of Covalent Hydrides:
- Down group: NH₃ > PH₃ > AsH₃ > SbH₃ > BiH₃
- Across period: CH₄ < NH₃ < H₂O < HF
▢ Metallic / Interstitial Hydrides:
- •Non-stoichiometric hydrides
- •Formed by d-block and f-block elements
- •Hydrogen atoms occupy interstitial sites in metal lattice
- •Strong reducing agents
- •Suggest hydrogen in atomic state
- •Example: ThH
▢ Polymeric Hydrides:
- •Formed by group 13 / boron family
- •Examples: B₂H₆, (AlH₃)n
▢ Complex Hydrides:
- LiAlH₄
- LiBH₄
- NaBH₄
Nitrogen Hydrides
Hydrides of nitrogen are basic except hydrazoic acid HN₃.
Reducing Nature
Hydrogen and hydrides act as reducing agents.
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PURIFICATION AND DRYING OF HYDROGEN
▢ Laboratory Purification:
Table 1: Impurity removal
Reagent | Removes |
|---|---|
AgNO₃ solution | PH₃, AsH₃ |
CuSO₄ solution | NH₃, H₂S |
Caustic soda / NaOH | CO₂, SO₂, NO₂ |
▢ Drying:
- •Moist H₂ dried by anhydrous CaCl₂
- •Moist H₂ dried by P₂O₅
▢ N₂ Contamination: Dry H₂ contaminated with N₂ is passed over heated Pd; Pd absorbs H₂ only and N₂ passes away.
▢ Hydrazoic Acid:
- •Hydrazoic acid + metal → azides
- •Azides used as blood preservatives and anticoagulants
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WATER
▢ Composition:
- •Gravimetric composition H : O = 1 : 8
- •Volumetric composition H : O = 2 : 1
- •Gravimetric composition established by Dumas
- •Water contains 8 parts oxygen and 1 part hydrogen by weight
▢ Physical Data:
Table 1: Water constants
Property | Value |
|---|---|
Dielectric constant | 81 |
Maximum density | 4°C |
Density at 4°C | 1 g/cc |
State | Liquid due to hydrogen bonding |
Dipole moment | 1.85 Debye |
▢ Structure:
- •Central atom → oxygen
- •Hybridisation of O → sp³
- •Shape → bent / V-shaped
- •Bond angle → 104.5°
- •Normal tetrahedral angle → 109°28′
- •Decrease in bond angle due to two lone pairs on oxygen
- •Water molecule is polar
▢ Density Anomaly:
- •Water has higher density than ice
- •Ice floats on water
- •Useful for aquatic life
- •Due to intermolecular hydrogen bonding and packing difference
▢ High Melting and Boiling Point:
- •Higher than hydrides of group VIA
- •Reason → hydrogen bonding
▢ Solvent Property:
- •Universal solvent
- •Leveling solvent
- •Polar inorganic solvent
- •Ionic compounds generally soluble
- •Solubility when hydration energy > lattice energy
- •Covalent compounds generally insoluble due to absence of hydrogen bonding
▢ Exceptions:
❖ Insoluble Ionic Compounds:
- AgCl
- BaSO₄
- CaF₂
❖ Soluble Organic Compounds:
- Alcohols
- Carboxylic acids
- Carbohydrates
❖ Reason: Hydrogen bonding with water
▢ Sterilization of Water:
- •Removal of harmful bacteria from drinking water
- •Methods → chlorination, boiling, ozonisation, aeration, UV rays
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HEAVY WATER
▢ Basic Facts:
- •Formula → D₂O
- •Also called → deuterium oxide
- •Discovered by Urey
- •Dielectric constant → 80.5
- •Temperature of maximum density → 11.6°C
- •NaCl is less soluble in heavy water than ordinary water
- •Ordinary water contains small fraction of heavy water
- •About 60 × 10³ L ordinary water contains nearly 1 L D₂O
▢ Comparison with Ordinary Water:
Table 1: H₂O vs D₂O
Property | H₂O | D₂O |
|---|---|---|
Freezing point | 0°C | 3.82°C |
Boiling point | 100°C | 101.42°C |
Density at 20°C | 0.9982 g/cc | 1.106 g/cc |
Temperature of maximum density | 4°C | 11.6°C |
Dielectric constant at 20°C | 82 | 80.5 |
▢ Recovery from Ordinary Water:
- Fractional distillation
- Prolonged electrolysis of ordinary water containing alkali
▢ Applications:
- •Moderator in nuclear reactor
- •Slows down neutrons
- •Used in medical science for isotopic study of cancer-affected tissue
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HARD AND SOFT WATER
▢ Hard Water:
- •Contains soluble salts of Ca²⁺ and Mg²⁺
- •Does not give lather with soap
- •Examples → sea water, river water, spring water
▢ Soft Water:
- •Pure water or water containing Na salts
- •Gives lather easily with soap
- •Examples → rain water, distilled water, demineralised water
▢ Hardness of Water:
❖ Cause: Soluble bicarbonates, chlorides and sulphates of calcium and magnesium.
❖ Distilled Water pH: pH < 7 due to atmospheric CO₂ forming H₂CO₃
▢ Types of Hardness:
Table 1: Temporary vs permanent hardness
Type | Cause | Heat effect |
|---|---|---|
Temporary hardness | Bicarbonates of Ca and Mg | Decomposes on heating |
Permanent hardness | Chlorides and sulphates of Ca and Mg | Stable to heat |
▢ Degree of Hardness:
- •Amount of hardness-causing substances in a given volume of water
- •Calculated as calcium carbonate equivalent
- •Expressed as ppm of CaCO₃
▢ Estimation: EDTA is used for estimation of hardness of water.
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REMOVAL OF HARDNESS
▢ Basic Principle: Precipitation or complex formation of Ca²⁺ and Mg²⁺ salts.
▢ Temporary Hardness Removal:
❖ Boiling:
- Ca(HCO₃)₂ → CaCO₃↓ + CO₂↑ + H₂O
❖ Clark's Method:
- Calculated quantity of slaked lime is added
- Ca(HCO₃)₂ + Ca(OH)₂ → 2CaCO₃↓ + 2H₂O
▢ Permanent Hardness Removal:
❖ Washing Soda Method:
- Washing soda removes both temporary and permanent hardness
- MgSO₄ + Na₂CO₃ → MgCO₃↓ + Na₂SO₄
❖ Soda-Lime Method: Removes both types of hardness.
❖ Calgon Process:
- •Based on formation of soluble complex
- •Calgon = sodium hexametaphosphate
- •Formula → Na₂[Na₄(PO₃)₆]
- •Ca²⁺ and Mg²⁺ form complex ions that do not precipitate with soap
❖ Calgon Reaction: Ca²⁺ + Na₂[Na₄(PO₃)₆] → 4Na⁺ + [Na₂Ca(PO₃)₆]²⁻
❖ Permutit Method:
- •Permutit = artificial zeolite
- •Also called sodium zeolite
- •Trade name of sodium aluminium orthosilicate
- •Formula → Na₂Al₂Si₂O₈·xH₂O
- •Exchanges Na⁺ with Ca²⁺ and Mg²⁺
- •10% NaCl brine regenerates exhausted permutit
❖ Permutit Reaction: Na₂Al₂Si₂O₈·xH₂O + MgCl₂ → MgAl₂Si₂O₈·xH₂O + 2NaCl
▢ High-Yield Notes:
- •Calgon removes hardness by soluble complex formation, not precipitation
- •Ion exchange resin method converts hard water into demineralised water
- •Permanent hardness removal methods also remove temporary hardness
- •Boiling and Clark's method remove only temporary hardness
- •AgCl, CaF₂ and BaSO₄ are water-insoluble ionic compounds
- •CaF₂ is also called John blue
- •Potash alum is used as water purifier
▢ Test of Water:
- •Anhydrous cobalt chloride: blue → pink on hydration
- •Anhydrous CuSO₄: white → blue on hydration
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HYDROGEN PEROXIDE
▢ Basic Facts:
- •Formula → H₂O₂
- •Also called → oxygenated water
- •Pale blue syrupy liquid
- •Diamagnetic
- •Prominent hydrogen bonding than water
- •Pure solution → weakly acidic
- •Aqueous solution → neutral
- •Antiseptic and germicide
- •Oxidising agent in laboratory
- •Used for bleaching substances
▢ Structure:
- •Non-planar molecule
- •All atoms do not lie in same plane
- •Open-book structure
▢ Preparation:
❖ From Hydrated Barium Peroxide:
- BaO₂·8H₂O + H₂SO₄ → BaSO₄↓ + H₂O₂ + 8H₂O
- H₃PO₄ is better than H₂SO₄ in laboratory preparation because it acts as negative catalyst for H₂O₂ decomposition
❖ Merck's Process:
- Na₂O₂ + H₂SO₄ → Na₂SO₄ + H₂O₂
- Calculated amount of sodium peroxide is added to 20% cold H₂SO₄
▢ Manufacture:
❖ Electrolysis of 50% H₂SO₄:
- After manufacture, acid concentration increases
- Cathode: 2H⁺ + 2e⁻ → 2H → H₂↑
- Anode: 2HSO₄⁻ → H₂S₂O₈ + 2e⁻
- H₂S₂O₈ = Marshall acid / peroxodisulphuric acid
- H₂S₂O₈ + 2H₂O → 2H₂SO₄ + H₂O₂
❖ Anthraquinol Process:
- 2-ethyl anthraquinol → 2-ethyl anthraquinone + H₂O₂
▢ Decomposition:
- •Unstable on standing or heating
- •2H₂O₂ → 2H₂O + O₂
- •Auto-oxidation reaction
- •Catalysed by Pt, Ag, Fe, Cu, MnO₂, Co
▢ Bleaching Action:
- •Dry bleach
- •Permanent bleaching
- •Oxidation process
▢ Acidic Property:
- •Can form peroxides
- •Acts as acid with bases
▢ Peroxide Formation:
- Na₂CO₃ + H₂O₂ → Na₂O₂ + H₂O + CO₂
- Ba(OH)₂ + H₂O₂ → BaO₂ + 2H₂O
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OXIDISING AND REDUCING PROPERTIES OF H₂O₂
▢ Oxidising Property:
- •Acts in acidic, alkaline and neutral medium
- •Dissociates to give H⁺ and hydroperoxide ion HO₂⁻
▢ H₂O₂ Oxidises:
- PbS → PbSO₄
- FeSO₄ → ferric salt
- KI → I₂
- Sodium arsenite → sodium arsenate
- Potassium ferrocyanide → potassium ferricyanide
▢ Oxidising Power Order: F₂ > atomic O > OF₂ > O₃ > H₂O₂ > KMnO₄ > K₂Cr₂O₇
▢ Reducing Property:
- •Acts in acidic, alkaline and neutral medium
- •Reduces halogens to halogen acids
- •Reduces potassium dichromate to chromium sulphate
- •Reduces ozone to oxygen in neutral medium
▢ Lead Paint Restoration:
❖ Concept: Old lead paint blackened by H₂S is restored by H₂O₂.
❖ Reaction: PbS + 4H₂O₂ → PbSO₄ + 4H₂O
❖ Colour Change: Black PbS → white PbSO₄
▢ Antichlor:
- •Substance that removes or dissolves Cl₂ left after bleaching
- •Examples → H₂O₂, SO₂, Na₂S₂O₃ solution
▢ Perhydrol:
- •30% aqueous H₂O₂ solution
- •Used as antiseptic
- •Used as mouth-washing liquid
- •Molarity → 8.8
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STORAGE, TEST AND CONCENTRATION OF H₂O₂
▢ Storage:
- •Stored in Teflon bottle or acid-proof plastic bottle
- •Paraffin wax layer used
- •Bottle surface should be smooth
- •Negative catalysts/inhibitors added → H₃PO₄, glycerol, acetanilide
- •Not stored in glass because alkaline oxides in glass catalyse decomposition
▢ Test:
- •In presence of FeSO₄, H₂O₂ turns starch iodide paper blue
- •In absence of FeSO₄, both H₂O₂ and O₃ turn starch iodide paper blue
▢ Volume Strength:
- •Expressed as volume of O₂ at NTP obtained by decomposition of 1 mL H₂O₂ solution
- •Volume strength = 5.6 × Normality
- •10 volume H₂O₂: 1 mL solution gives 10 mL O₂ at NTP
- •20 volume H₂O₂: 1 mL solution gives 20 mL O₂ at NTP
▢ Equivalent Weight: Equivalent weight of H₂O₂ = 17
▢ Important Relations:
- 10 volume H₂O₂ = 3.035% H₂O₂
- 10 volume H₂O₂ = 30.35 g/L H₂O₂
- 10 volume H₂O₂ = 1.75 N
- 10 volume H₂O₂ ≈ 1.79 N
- 30 volume H₂O₂ ≈ 5.35–5.37 N
▢ Numerical Facts:
- •1 L of 2 M H₂O₂ contains 68 g H₂O₂
- •100 mL of 2 M H₂O₂ contains 6.8 g H₂O₂
- •Complete decomposition of 100 mL of 2 M H₂O₂ gives 2.24 L O₂ at STP
- •30 volume H₂O₂ contains about 91.07 g/L H₂O₂
📚
HYDRATES AND WATER OF CRYSTALLIZATION
▢ Types of Hydrates:
Table 1: Hydrates
Type | Meaning | Example |
|---|---|---|
Cationic hydrates | Water molecules held by cations | MgCl₂·6H₂O, CaCl₂·6H₂O |
Lattice hydrates | Water molecules held in lattice sites | Na₂CO₃·10H₂O |
Anionic hydrates | Water molecules held by anions and cations | CuSO₄·5H₂O, MgSO₄·7H₂O |
▢ Absorption and Loss of Water:
Table 1: Water absorption/loss
Term | Meaning | Examples |
|---|---|---|
Hygroscopic | Absorb moisture from air | NH₄NO₃ |
Deliquescent | Absorb large amount of water and dissolve | NaOH, CaCl₂, NaNO₃ |
Efflorescent | Lose water of crystallization | CaSO₄·2H₂O, CuSO₄·5H₂O, MgSO₄·7H₂O, FeSO₄·7H₂O |
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SOAPS AND DETERGENTS
▢ Soaps:
- •Sodium or potassium salts of higher fatty acids
- •Sodium salts → hard soap / washing soap
- •Potassium salts → soft soap / bath soap
- •Process of soap formation → saponification
- •Soaps of metals other than Na or K are usually insoluble in water
- •Dirt is removed by action of water on soap
▢ Synthetic Detergents:
- •Also called soapless soaps or syndets
- •May or may not be biodegradable
- •Common group → R–O–SO₃–Na
▢ Types of Synthetic Detergents:
- Sodium alkyl sulphates, e.g. sodium lauryl sulphate
- Sodium alkyl aryl sulphonates, e.g. sodium dodecyl benzene sulphonate
📚
READ AND DIGEST POINTS
▢ Hydrogen and Water:
- •Two ice cubes pressed together form a single cube due to hydrogen bonding
- •Ozone purifies water by destroying viruses and bacteria
- •Sea water can be purified by reverse osmosis
- •Non-metallic character of H₂O distinguishes it from alkali metals
- •Hydrogen has negative valency in NaH
- •Surface water contains salts and organic matter
- •AgI is used for artificial rain
- •0.9% NaCl solution is isotonic with human blood
- •Zeolite is a silicate compound
- •Sodium catches fire with water due to burning of H₂
▢ Hydrogen Peroxide:
- •H₂O₂ is neutral, but commercial H₂O₂ is acidic
- •Aqueous H₂O₂ is neutral
- •H₂O₂ is better oxidising agent than reducing agent
- •H₂O₂ shows auto-oxidation
- •H₂O₂ oxidises MnSO₄ to MnO₂ in alkaline medium
- •H₂O₂ oxidises KNO₂ to KNO₃ in neutral medium
- •H₂O₂ reduces O₃ to O₂ in neutral medium
- •H₂O₂ is not stored in glass because alkaline oxides in glass catalyse decomposition
- •Decomposition of H₂O₂ is slowed by alcohol
- •Reaction of H₂O₂ with H₂S is a redox reaction
- •Decomposition of H₂O₂ is favoured by MnO₂
- •2H₂O₂ → 2H₂O + O₂ shows decomposition of H₂O₂
- •Industrial preparation of H₂O₂ is generally by electrolysis of 50% H₂SO₄
- •H₂O₂ used as rocket fuel at about 90% concentration
- •H₂O₂ is used for bleaching hair
▢ Addition Reaction of H₂O₂: CH₂=CH₂ + H₂O₂ → HO–CH₂–CH₂–OH
Q1.
Which of the following doesn't displace hydrogen?
📅IOM 2066
Q2.
A deuteron contains
📅MOE
Q3.
Ortho and para hydrogen differ in
📅I.E.
Q4.
Hydrogen, deuterium and tritium have
📅MOE
Q5.
In preparation of vanaspati ghee, the reaction involving hydrogen is called
📅IOE/MOE
Q6.
Hydrogen forms
📅IOE
Q7.
The most reactive form of hydrogen is
📅I.E.
Q8.
Ortho and para forms of hydrogen can be separated by
📅I.E.
Q9.
Lane's process is for
📅K.U.
Q10.
Atomic hydrogen produces formaldehyde when it reacts with
📅IOM 2004
Q11.
Hydrogen cannot be obtained by
📅IOM 2005
Q12.
Hydrogen burns in air with a
📅MOE
Q13.
Which particle is emitted by tritium?
📅I.E.
Q14.
Which has equal no. of neutrons and protons?
📅BPKIHS 2005
Q15.
H loses electron to form H⁺. In this aspect H behaves as
📅MOE 2008
Q16.
Finely divided nickel is used as a catalyst in
📅MOE 2050
Q17.
Which is reduced by H₂?
📅MOE 2069
Q18.
Hydrogen differs from halogens in
📅Bangladesh, Embassy 2001
Q19.
Which contains acidic hydrogen atom?
📅K.U. 2004
Q20.
NaI is an example of
📅I.E. 2001
Q21.
The gas used in sterilizing water is
📅MOE 2066
Q22.
Heavy water is used as
📅BPKIHS
Q23.
Maximum hydrogen bonds a water molecule can form is
📅BPKIHS
Q24.
Which produces hard water?
Q25.
Calgon's process uses
📅MOE
Q26.
Best method to test water presence?
📅MOE, IOM 1998
Q27.
High density of water vs ice is due to
📅MOE
Q28.
A hydrated salt losing water in air is called
📅MOE
Q29.
Calgon is
📅MOE/IOM 2004
Q30.
Water is
📅IOM 1994
Q31.
A dilute H₂O₂ solution can be concentrated by
Q32.
Fenton's reagent is
📅BPKIHS
Q33.
The oxide that gives H₂O₂ with dilute acid is
📅BPKIHS
Q34.
Moderator in nuclear reactor is
📅BPKIHS
Q35.
H₂S + H₂O₂ → S + H₂O shows
📅MOE
Q36.
Volume strength of 1.5 N H₂O₂ is
Q37.
H₂O₂ acts as oxidizing agent with
📅BPKIHS
Q38.
Permanent hardness is due to
📅BPKIHS
Q39.
Calgon process involves
📅MOE 2003
Q40.
Acid rain doesn't contain
📅MOE 2060
Q41.
Which is correct?
📅MOE 2050