Surface Chemistry Class 12th Notes - Free NCERT Class 12 chemistry Chapter 5 Notes - Download PDF

Surface Chemistry Class 12th Notes - Free NCERT Class 12 chemistry Chapter 5 Notes - Download PDF

Edited By Sumit Saini | Updated on Apr 22, 2022 04:00 PM IST

The chapter, surface chemistry is the continuation of the NCERT chapter, chemical kinetics. The ncert Class 12 Chemistry chapter 5 notes covers a brief profile of the surface chemistry chapter. The main topics covered in Class 12 Chemistry chapter 5 notes are mechanism of adsorption, introduction to adsorption, adsorption isotherms, the difference between absorption and adsorption, types of adsorption, adsorption from solution phase, applications of adsorption.

This Story also Contains
  1. Surface Chemistry :
  2. Surface Chemistry Class 12 Notes - Topic 1:
  3. Adsorption:
  4. NCERT Class 12 Chemistry Chapter 5 Notes- Topic 2:
  5. Catalysis:
  6. Surface Chemistry Class 12 Notes- Topic 3:
  7. Colloids:
  8. NCERT Class 12 Chemistry Chapter 5 Notes - Topic 4
  9. Emulsions:
  10. NCERT Class 12 Notes Chapter-Wise
  11. NCERT Books and Syllabus

NCERT Class 12 Chemistry chapter 5 notes also include a brief introduction to catalysis, types of catalysis, adsorption theory of heterogeneous catalysis, enzyme catalysis. Class 12 Chemistry chapter 5 notes also cover the basic equations in the chapter. The basics of colloids, classification of colloids, preparations of colloids, purification of colloids, properties of colloids, and emulsions are also covered in the CBSE Class 12 Chemistry chapter 5 notes. These Surface Chemistry Class 12 notes also include some solved examples related to mentioned topics. All these topics can be downloaded from Class 12 Chemistry chapter 5 notes pdf download.

Also, students can refer,

Surface Chemistry :

The branch of chemistry that deals with surface/interface occurring phenomenon is called surface chemistry. The bulk phases can be liquid or solid. There is no existence of interface in gases due to their complete miscibility with other gases.

Surface Chemistry Class 12 Notes - Topic 1:

Adsorption:

The phenomenon of accumulation or retention of molecular species on the surface of solids or liquids rather than in bulk is known as adsorption.

  • Adsorbate - The substance which accumulates or retains at the surface is called adsorbate.

  • Adsorbent - The substance on which adsorbate accumulates is called adsorbent. For example - alumina gel, charcoal, silica gel, colloids, clay, etc.

Desorption:

The phenomenon in which adsorbate is removed from the adsorbent is called desorption. It is the opposite of adsorption.

Difference Between Absorption and Adsorption:

Absorption

Adsorption

The phenomenon of assimilation in which the constituent of a substance enters into the bulk phase of another substance.

The phenomenon in which the adhesion of constituents of a substance takes place on the surface of another substance.


Bulk phenomenon

Surface phenomenon

Uniform distribution of absorbate

Adsorbate concentrates only on the surface

Endothermic process

Exothermic process

Independent of temperature

Temperature-dependent

The rate of reaction is uniform for absorption

The rate of reaction increases slowly and then achieves equilibrium.

Example- absorption of liquid by a sponge.

Example- adsorption of pollutants by pollution masks.

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Mechanism of adsorption:

  1. The surface constituents of the adsorbent are in a different environment than the bulk constituents.

  2. The forces acting between bulk constituent and its neighbors are mutually balanced.

  3. The forces exerted by surface constituents are unbalanced and thus called residual forces.

  4. Residual forces attract the particles of adsorbate towards the surface of the adsorbent.

  5. At a given temperature and pressure, the increase of surface area per unit mass of the adsorbent increases the extent of adsorption.

  6. ΔH is negative, ΔS is negative and thus ΔG is negative.

Types of adsorption :

There are two types of adsorption on the basis of the type of forces acting between constituents.

Physisorption

Chemisorption

Arises due to Van Der Waal’s forces

Arises due to the formation of chemical bonds

Non-specific in nature

Highly specific in nature

Reversible

Irreversible

Depends on the nature of gas

Depends on the nature of gas

Low enthalpy of adsorption

High enthalpy of adsorption

Low temperature is favorable

High temperature is favorable

No appreciable activation energy needed

Sometimes high activation energy is needed

Depends on the surface area

Depends on the surface area

Multimolecular layers are formed

The unimolecular layer is formed

Adsorption isotherms :

At constant temperature, the variation of the amount of gas adsorbed by the adsorbent with pressure is expressed via adsorption isotherms.

  • Freundlich adsorption isotherm:

The quantity of gas adsorbed by unit mass of solid adsorbent and pressure at a particular temperature is expressed as:

<math xmlns="http://www.w3.org/1998/Math/MathML"><mfrac><mi>x</mi><mi>m</mi></mfrac><mo>=</mo><mi>k</mi><mo>.</mo><msup><mi>p</mi><mfrac bevelled="true"><mn>1</mn><mi>n</mi></mfrac></msup><mo> </mo><mfenced><mrow><mi>n</mi><mo>></mo><mn>1</mn></mrow></mfenced></math>

x - the mass of gas adsorbate

m - the mass of adsorbent

p - pressure

n & k - constants that depend on the nature of the adsorbent & the gas at a particular temperature

1645006183723

Take log on both sides :

<math xmlns="http://www.w3.org/1998/Math/MathML"><mi>log</mi><mfrac><mi>x</mi><mi>m</mi></mfrac><mo>=</mo><mi>log</mi><mo> </mo><mi>k</mi><mo> </mo><mo>+</mo><mo> </mo><mfrac><mn>1</mn><mi>n</mi></mfrac><mi>log</mi><mo> </mo><mi>p</mi><mo> </mo></math>

On comparing with y = mx + c,

y = log (x/m)

m = 1/n

x = log p

c = log k

The graph for Freundlich isotherm can be plotted as below:

1645006180911

Adsorption from solution phase

Solids can also adsorb solutes from solutions. Some observations from solid-liquid adsorption are given below:

  1. As temperature increases ↑ the extent of adsorption decreases ↓

  2. As the surface area of the adsorbent increases ↑ the extent of adsorption increases ↑

  3. The extent of adsorption is dependant on the concentration of solute.

  4. The extent of adsorption is dependant on the nature of adsorbate and adsorbent.

Freundlich equation for adsorption from solution by solid adsorbate:

<math xmlns="http://www.w3.org/1998/Math/MathML"><mfrac><mi>x</mi><mi>m</mi></mfrac><mo>=</mo><mi>k</mi><msup><mi>C</mi><mfrac bevelled="true"><mn>1</mn><mi>n</mi></mfrac></msup></math>

Take log on both sides :

<math xmlns="http://www.w3.org/1998/Math/MathML"><mi>log</mi><mfrac><mi>x</mi><mi>m</mi></mfrac><mo>=</mo><mi>log</mi><mo> </mo><mi>k</mi><mo> </mo><mo>+</mo><mfrac><mn>1</mn><mi>n</mi></mfrac><mi>log</mi><mo> </mo><mi>C</mi></math>

Comparing the above equation with y = mx+c we get a straight line graph.

Applications of adsorption :

Gas masks, Heterogeneous catalysis, Removal of coloring matter from solutions, Separation of inert gases, In curing diseases, Froth floatation process, Control of humidity, Adsorption indicators, Production of high vacuum, Chromatographic analysis, etc.

NCERT Class 12 Chemistry Chapter 5 Notes- Topic 2:

Catalysis:

The process of altering the rate of reaction of a chemical reaction by introducing a catalyst.

Catalysts are substances that accelerate or decelerate the rate of a reaction and is retrieved unchanged after the completion of the reaction.

  • Promoters: Enhance activity of the catalyst

  • Poisons: Diminish activity of the catalyst

Classification of catalysis:

  • Homogeneous catalysis: The catalysis in which both reactants and catalyst(s) are in the same phase. Examples -

  • Oxidation of sulfur dioxide

<math xmlns="http://www.w3.org/1998/Math/MathML"><mn>2</mn><msub><mi>SO</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mo>+</mo><msub><mi mathvariant="normal">O</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mover><mo>→</mo><mrow><mi>NO</mi><mfenced><mi mathvariant="normal">g</mi></mfenced></mrow></mover><mn>2</mn><msub><mi>SO</mi><mn>3</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced></math>

  • Hydrolysis of methyl acetate

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi>CH</mi><mn>3</mn></msub><msub><mi>COOCH</mi><mn>3</mn></msub><mfenced><mi mathvariant="normal">l</mi></mfenced><mo>+</mo><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mfenced><mi mathvariant="normal">l</mi></mfenced><mover><mo>→</mo><mrow><mi>HCl</mi><mfenced><mi mathvariant="normal">l</mi></mfenced></mrow></mover><msub><mi>CH</mi><mn>3</mn></msub><mi>COOH</mi><mfenced><mi>aq</mi></mfenced><mo> </mo><mo>+</mo><mo> </mo><msub><mi>CH</mi><mn>3</mn></msub><mi>OH</mi><mfenced><mi>aq</mi></mfenced></math>

  • Hydrolysis of sugar

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi mathvariant="normal">C</mi><mn>12</mn></msub><msub><mi mathvariant="normal">H</mi><mn>22</mn></msub><msub><mi mathvariant="normal">O</mi><mn>11</mn></msub><mfenced><mi>aq</mi></mfenced><mo>+</mo><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mfenced><mi mathvariant="normal">l</mi></mfenced><mover><mo>→</mo><mrow><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><msub><mi>SO</mi><mn>4</mn></msub><mfenced><mi mathvariant="normal">l</mi></mfenced></mrow></mover><msub><mi mathvariant="normal">C</mi><mn>6</mn></msub><msub><mi mathvariant="normal">H</mi><mn>12</mn></msub><msub><mi mathvariant="normal">O</mi><mn>6</mn></msub><mo> </mo><mfenced><mi>aq</mi></mfenced><mo> </mo><mo>+</mo><mo> </mo><msub><mi mathvariant="normal">C</mi><mn>6</mn></msub><msub><mi mathvariant="normal">H</mi><mn>12</mn></msub><msub><mi mathvariant="normal">O</mi><mn>6</mn></msub><mo> </mo><mfenced><mi>aq</mi></mfenced></math>

  • Heterogeneous catalysis: The catalysis in which both reactants and catalyst(s) are in different phases. Examples -

  • Oxidation of sulfur dioxide

<math xmlns="http://www.w3.org/1998/Math/MathML"><mn>2</mn><msub><mi>SO</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mover><mo>→</mo><mrow><mi>Pt</mi><mfenced><mi mathvariant="normal">s</mi></mfenced></mrow></mover><mn>2</mn><msub><mi>SO</mi><mn>3</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced></math>

  • Haber’s Process

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi mathvariant="normal">N</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mo>+</mo><mn>3</mn><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mover><mo>→</mo><mrow><mi>Fe</mi><mfenced><mi mathvariant="normal">s</mi></mfenced></mrow></mover><mn>2</mn><msub><mi>NH</mi><mn>3</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced></math>

  • Ostwald’s process

<math xmlns="http://www.w3.org/1998/Math/MathML"><mn>4</mn><msub><mi>NH</mi><mn>3</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mo>+</mo><mn>5</mn><msub><mi mathvariant="normal">O</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mover><mo>→</mo><mrow><mi>Pt</mi><mfenced><mi mathvariant="normal">s</mi></mfenced></mrow></mover><mn>4</mn><mi>NO</mi><mfenced><mi mathvariant="normal">g</mi></mfenced><mo>+</mo><mn>6</mn><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mfenced><mi mathvariant="normal">l</mi></mfenced></math>

  • Hydrogenation of vegetable oil

<math xmlns="http://www.w3.org/1998/Math/MathML"><mi>Vegetable</mi><mo> </mo><mi>oil</mi><mo> </mo><mfenced><mi mathvariant="normal">l</mi></mfenced><mo>+</mo><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mover><mo>→</mo><mrow><mi>Ni</mi><mfenced><mi mathvariant="normal">s</mi></mfenced></mrow></mover><mi>Vegetable</mi><mo> </mo><mi>ghee</mi><mfenced><mi mathvariant="normal">s</mi></mfenced></math>

Adsorption theory of heterogeneous catalysis:

The adsorption theory of heterogeneous catalysis explains the mechanism of heterogeneous catalysis. The mechanism can be explained in 5 steps:

  1. Reactants diffuse on the surface of the catalyst.

  2. Reactant molecules get adsorbed on the surface of the catalyst.

  3. A chemical reaction occurs via the formation of an intermediate.

  4. Reaction products are desorbed from the surface of the catalyst.

  5. Diffusion of products away from the surface of the catalyst.

This adsorption theory gives an explanation for the unchanged composition of catalyst at the end of the reaction.

1645006176129

Shape selective catalysis by zeolites:

Shape-selective catalysis is a catalytic reaction in which the pore structure of the catalyst and the size of the reactant and product molecules are major factors to carry out the reaction.

Due to their honeycomb-like structures, zeolites are good shape-selective catalysts.

Zeolites are microporous aluminosilicates with a 3D network of silicates in which sometimes aluminium atoms replace silicon atoms giving an Al-O-si framework.

Enzyme catalysis:

Enzymes are proteins of high molecular mass. They form colloidal solutions in water. They are very effective catalysts in natural processes. Enzymes are also called biochemical catalysts. Enzyme catalyzed reactions are also called biochemical catalysis. Some examples are discussed below:

  1. Inversion of cane sugar

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi mathvariant="normal">C</mi><mn>12</mn></msub><msub><mi mathvariant="normal">H</mi><mn>22</mn></msub><msub><mi mathvariant="normal">O</mi><mn>11</mn></msub><mo> </mo><mfenced><mi>aq</mi></mfenced><mo>+</mo><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mfenced><mi mathvariant="normal">l</mi></mfenced><mover><mo>→</mo><mi>Inverse</mi></mover><msub><mi mathvariant="normal">C</mi><mn>6</mn></msub><msub><mi mathvariant="normal">H</mi><mn>12</mn></msub><msub><mi mathvariant="normal">O</mi><mn>6</mn></msub><mfenced><mi>aq</mi></mfenced><mo>+</mo><mo> </mo><msub><mi mathvariant="normal">C</mi><mn>6</mn></msub><msub><mi mathvariant="normal">H</mi><mn>12</mn></msub><msub><mi mathvariant="normal">O</mi><mn>6</mn></msub><mfenced><mi>aq</mi></mfenced><mspace linebreak="newline"></mspace><mspace linebreak="newline"></mspace></math>

  1. Conversion of glucose into ethyl alcohol

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi mathvariant="normal">C</mi><mn>6</mn></msub><msub><mi mathvariant="normal">H</mi><mn>12</mn></msub><msub><mi mathvariant="normal">O</mi><mn>6</mn></msub><mo> </mo><mfenced><mi>aq</mi></mfenced><mover><mo>→</mo><mi>Zymase</mi></mover><mn>2</mn><msub><mi mathvariant="normal">C</mi><mn>2</mn></msub><msub><mi mathvariant="normal">H</mi><mn>5</mn></msub><mi>OH</mi><mfenced><mi>aq</mi></mfenced><mo> </mo><mo>+</mo><mn>2</mn><msub><mi>CO</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced></math>

  1. ‘Conversion of starch into maltose

<math xmlns="http://www.w3.org/1998/Math/MathML"><mn>2</mn><msub><mfenced><mrow><msub><mi mathvariant="normal">C</mi><mn>6</mn></msub><msub><mi mathvariant="normal">H</mi><mn>10</mn></msub><msub><mi mathvariant="normal">O</mi><mn>5</mn></msub></mrow></mfenced><mi mathvariant="normal">n</mi></msub><mo> </mo><mfenced><mi>aq</mi></mfenced><mo>+</mo><msub><mi>nH</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mfenced><mi mathvariant="normal">l</mi></mfenced><mover><mo>→</mo><mi>Diastase</mi></mover><msub><mi>nC</mi><mn>12</mn></msub><msub><mi mathvariant="normal">H</mi><mn>22</mn></msub><msub><mi mathvariant="normal">O</mi><mn>11</mn></msub><mfenced><mi>aq</mi></mfenced></math>

  1. Conversion of maltose into glucose

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi mathvariant="normal">C</mi><mn>12</mn></msub><msub><mi mathvariant="normal">H</mi><mn>22</mn></msub><msub><mi mathvariant="normal">O</mi><mn>11</mn></msub><mfenced><mi>aq</mi></mfenced><mo>+</mo><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mfenced><mi mathvariant="normal">l</mi></mfenced><mover><mo>→</mo><mi>Maltase</mi></mover><mn>2</mn><msub><mi mathvariant="normal">C</mi><mn>6</mn></msub><msub><mi mathvariant="normal">H</mi><mn>12</mn></msub><msub><mi mathvariant="normal">O</mi><mn>6</mn></msub><mfenced><mi>aq</mi></mfenced></math>

  1. Decomposition of urea into ammonia and carbon dioxide

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi>NH</mi><mn>2</mn></msub><msub><mi>CONH</mi><mn>2</mn></msub><mfenced><mi>aq</mi></mfenced><mo>+</mo><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mfenced><mi mathvariant="normal">l</mi></mfenced><mover><mo>→</mo><mi>Urease</mi></mover><mn>2</mn><msub><mi>NH</mi><mn>3</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced><mo>+</mo><msub><mi>CO</mi><mn>2</mn></msub><mfenced><mi mathvariant="normal">g</mi></mfenced></math>

A short summary of enzyme-catalyzed reactions is tabulated below:

1645006174957

Characteristics of enzyme catalysis:

  1. Highly efficient

  2. Highly specific in nature

  3. Highly active under optimum temperature (298-310K)

  4. Highly active under optimum pH (5-7)

  5. Increased activity in the presence of activators & co-enzymes

  6. Decreased activity due to influence of inhibitors and poisons

Mechanism of enzyme catalysis:

Step 1: Enzyme binds to substrate to form an activated complex.

<math xmlns="http://www.w3.org/1998/Math/MathML"><mi>E</mi><mo> </mo><mo>+</mo><mo> </mo><mi>S</mi><mo> </mo><mo>→</mo><mi>E</mi><msup><mi>S</mi><mo>≠</mo></msup></math>

Step 2: Activated complex is decomposed to form the product.

<math xmlns="http://www.w3.org/1998/Math/MathML"><msup><mi>ES</mi><mo>≠</mo></msup><mo>→</mo><mi mathvariant="normal">E</mi><mo> </mo><mo>+</mo><mo> </mo><mi mathvariant="normal">P</mi></math>

1645006185109

Surface Chemistry Class 12 Notes- Topic 3:

Colloids:

A heterogeneous system in which very fine particles of one substance called dispersed phase is dispersed in another substance is termed as the dispersion medium.

Classification of colloids:

Colloids can be classified on the basis of:

  • Physical state

  • Nature of interaction

  • Type of particles

Classification based on the physical state of the dispersed phase and dispersion medium:

Dispersed phase

Dispersion medium

Type of colloid

Examples

Solid

Solid

Solid sol

Colored glass, gemstones

Solid

Liquid

Sol

Paints, cell fluids

Solid

Gas

Aerosol

Smoke, dust

Liquid

Solid

Gel

Cheese, butter, jellies

Liquid

Liquid

Emulsion

Milk, hair cream

Liquid

Gas

Aerosol

Fog, mist, cloud, insecticide sprays

Gas

Solid

Solid sol

Pumice stone, foam rubber

Gas

Liquid

Foam

Froth, whipped cream, soap lather

Classification based on the nature of the interaction between the dispersion medium and dispersed phase:

Colloids can be classified on the basis of interaction in 2 categories:

Property

Lyophobic

Lyophilic

Preparation

Can not be prepared easily

Can be prepared easily

Stability

Less stable

More stable

Reversibility

Irreversible

Reversible

Viscosity

Nearly the same viscosity as the solvent

Higher viscosity than solvent

Surface tension

Nearly the same surface tension as a solvent

Higher surface tension than solvent

Hydration / solvation

Less solvated

Highly solvated

Charge

Positive / negative

No charge

Visibility

Can be seen under a microscope

Can not be seen under a microscope

Coagulation/Precipitation

Precipitated by low concentration of electrolytes

Precipitated by high concentration of electrolytes

Tyndall effect

More scattering

Less scattering

Migration in an electric field

Migrate towards cathode/anode

May/ may not migrate

Nature

Mostly inorganic

Mostly organic

Classification based on the type of particles of the dispersed phase and dispersion medium:

Multimolecular colloids: On dissolution, a large number of atoms and smaller molecules aggregate to form colloidal species called multimolecular colloids.

Multimolecular colloids: In suitable solvents, macromolecules forms colloidal solutions.

Associated colloids: substances that act as normal strong electrolytes at low concentration but show colloidal behavior at high concentration due to the formation of aggregate molecules called micelles.

Kraft temperature - temperature above which micelle formation takes place.

Critical micelle concentration - concentration above which micelle formation takes place.

Micelle formation and cleansing action of soap -

  1. Micelle consists of a hydrophobic hydrocarbon–like central core.

  2. Soap molecules form micelle around the oil droplet.

  3. The hydrophobic part of the stearate ions is in the oil droplet and the hydrophilic part extends out of the droplet.

  4. The polar groups interact with water.

  5. The oil droplet surrounded pulled in water and removed from the dirty surface.

  6. Soap helps in emulsification and washing away of oils & dirt.

  7. The negatively charged sheath around the oil droplets prevents them from aggregating.

Preparation of colloids:

  • Chemical methods

Molecules formed by chemical reactions aggregate to form sols. Example-

<math xmlns="http://www.w3.org/1998/Math/MathML"><msub><mi>FeCl</mi><mn>3</mn></msub><mo> </mo><mo>+</mo><mo> </mo><mn>3</mn><msub><mi mathvariant="normal">H</mi><mn>2</mn></msub><mi mathvariant="normal">O</mi><mover><mo>→</mo><mi>Hydrolysis</mi></mover><mi>Fe</mi><msub><mfenced><mi>OH</mi></mfenced><mn>3</mn></msub><mfenced><mi>sol</mi></mfenced><mo>+</mo><mn>3</mn><mi>HCl</mi></math>

Electrical disintegration or Bredig’s Arc method

The intense heat produced between the electrodes vapourises the metal. This metal then condenses to form particles of colloidal size.

Peptization

The process of converting a precipitate in the presence of a small amount of electrolyte into colloidal sol by shaking it with a dispersion medium is called peptization.

Purification of colloidal solutions:

Purification can be done by (These processes are not discussed in detail in class 12 chemistry chapter 5 notes.) :

  1. Dialysis

  2. Electrodialysis

  3. Ultrafiltration

Properties of colloidal solution:

  1. colligative properties are of small order than true solutions.

  2. Tyndall effect - Colloidal solutions show a mild to strong opalescence when viewed at right angles to the passage of light.

  3. Colour - the color of the colloidal solution changes with the perspective of the viewer.

  4. Brownian movement - the state of continuous zig-zag motion.

  5. A charge is always present on colloidal particles.

  6. Electrophoresis.

  7. Coagulation and precipitation.

NCERT Class 12 Chemistry Chapter 5 Notes - Topic 4

Emulsions:

Emulsions are formed by the dispersion of finely divided droplets of one liquid in another liquid. They are liquid-liquid colloidal systems.

Types of emulsions:

Oil-in-water: In this system, water is a dispersion medium, and oil is a dispersed phase. Example - butter.

Water-in-oil: In this system, oil is a dispersion medium, and water is a dispersed phase.

Emulsifying agent - A substance that forms an interfacial film between the dispersed phase and dispersed medium.

Applications of colloids:

  1. Electrical precipitation of smoke

  2. Purification of drinking water

  3. Medicines

  4. Tanning

  5. The cleansing action of soap

  6. Photographic films

  7. Rubber industry

  8. Industrial Products

Significance of NCERT Class 12 Chemistry chapter 5 notes

surface chemistry Class 12 notes will be helpful to revise the chapter and to get an idea about the main topics covered in the chapter. Also, this ncert class 12 chemistry chapter 5 notes are useful to cover the main topics of the Class 12 CBSE Chemistry syllabus and also for competitive exams like VITEEE, BITSAT, JEE Main, NEET, etc. Class 12 Chemistry chapter 5 notes pdf download can be used to prepare in offline mode.

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A block of mass 0.50 kg is moving with a speed of 2.00 ms-1 on a smooth surface. It strikes another mass of 1.00 kg and then they move together as a single body. The energy loss during the collision is

Option 1)

0.34\; J

Option 2)

0.16\; J

Option 3)

1.00\; J

Option 4)

0.67\; J

A person trying to lose weight by burning fat lifts a mass of 10 kg upto a height of 1 m 1000 times.  Assume that the potential energy lost each time he lowers the mass is dissipated.  How much fat will he use up considering the work done only when the weight is lifted up ?  Fat supplies 3.8×107 J of energy per kg which is converted to mechanical energy with a 20% efficiency rate.  Take g = 9.8 ms−2 :

Option 1)

2.45×10−3 kg

Option 2)

 6.45×10−3 kg

Option 3)

 9.89×10−3 kg

Option 4)

12.89×10−3 kg

 

An athlete in the olympic games covers a distance of 100 m in 10 s. His kinetic energy can be estimated to be in the range

Option 1)

2,000 \; J - 5,000\; J

Option 2)

200 \, \, J - 500 \, \, J

Option 3)

2\times 10^{5}J-3\times 10^{5}J

Option 4)

20,000 \, \, J - 50,000 \, \, J

A particle is projected at 600   to the horizontal with a kinetic energy K. The kinetic energy at the highest point

Option 1)

K/2\,

Option 2)

\; K\;

Option 3)

zero\;

Option 4)

K/4

In the reaction,

2Al_{(s)}+6HCL_{(aq)}\rightarrow 2Al^{3+}\, _{(aq)}+6Cl^{-}\, _{(aq)}+3H_{2(g)}

Option 1)

11.2\, L\, H_{2(g)}  at STP  is produced for every mole HCL_{(aq)}  consumed

Option 2)

6L\, HCl_{(aq)}  is consumed for ever 3L\, H_{2(g)}      produced

Option 3)

33.6 L\, H_{2(g)} is produced regardless of temperature and pressure for every mole Al that reacts

Option 4)

67.2\, L\, H_{2(g)} at STP is produced for every mole Al that reacts .

How many moles of magnesium phosphate, Mg_{3}(PO_{4})_{2} will contain 0.25 mole of oxygen atoms?

Option 1)

0.02

Option 2)

3.125 × 10-2

Option 3)

1.25 × 10-2

Option 4)

2.5 × 10-2

If we consider that 1/6, in place of 1/12, mass of carbon atom is taken to be the relative atomic mass unit, the mass of one mole of a substance will

Option 1)

decrease twice

Option 2)

increase two fold

Option 3)

remain unchanged

Option 4)

be a function of the molecular mass of the substance.

With increase of temperature, which of these changes?

Option 1)

Molality

Option 2)

Weight fraction of solute

Option 3)

Fraction of solute present in water

Option 4)

Mole fraction.

Number of atoms in 558.5 gram Fe (at. wt.of Fe = 55.85 g mol-1) is

Option 1)

twice that in 60 g carbon

Option 2)

6.023 × 1022

Option 3)

half that in 8 g He

Option 4)

558.5 × 6.023 × 1023

A pulley of radius 2 m is rotated about its axis by a force F = (20t - 5t2) newton (where t is measured in seconds) applied tangentially. If the moment of inertia of the pulley about its axis of rotation is 10 kg m2 , the number of rotations made by the pulley before its direction of motion if reversed, is

Option 1)

less than 3

Option 2)

more than 3 but less than 6

Option 3)

more than 6 but less than 9

Option 4)

more than 9

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