(i) At 298 K the volume of `NH_(3)` adsorbed by 1 g of charcoal is higher than that of `H_(2)` under similar conditions.
(ii) The movement of colloidal particles towards the oppositely charged electrodes on passing current is known as Brownian movement.
If T for true and F for false then correct option is :
(i) At 298 K the volume of `NH_(3)` adsorbed by 1 g of charcoal is higher than that of `H_(2)` under similar conditions.
(ii) The movement of colloidal particles towards the oppositely charged electrodes on passing current is known as Brownian movement.
If T for true and F for false then correct option is :
(ii) The movement of colloidal particles towards the oppositely charged electrodes on passing current is known as Brownian movement.
If T for true and F for false then correct option is :
A
T,T
B
T,F
C
F,T
D
F,F
Text Solution
AI Generated Solution
To solve the question, we need to evaluate the two statements provided and determine whether they are true (T) or false (F).
### Step 1: Analyze the first statement
The first statement is: "At 298 K the volume of `NH3` adsorbed by 1 g of charcoal is higher than that of `H2` under similar conditions."
1. **Understand the concept of adsorption**: Adsorption is the process where molecules adhere to a surface. The extent of adsorption can depend on various factors, including the critical temperature of the gas.
2. **Identify the critical temperatures**:
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The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. Under the influence of an electric field, the particles in a sol migrate towards cathode. The coagulation of the same sol is studied using NaCl, Na_(2)SO_(4) and Na_(3)PO_(4) solutions. Their coagulating values will be in the order :
The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. How would you obtain a sol of AgI, the particles of which migrate towards cathode under the electric field?
The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. A gelatin sol at pH less than the isoelectric value is subjected to an electric field. The sol particles migrate toward :
The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. 100 ml each of two sols of AgI, one obtained by adding AgNO_(3) to slight excess of KI and another obtained by adding KI to slight excess of AgNO_(3) , are mixed together. Then :
The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. Which of the following ions would have the minimum coagulating value for sol obtained on peptizing Sn(OH)_(4) by little NaOH solution?
N_(2)(g)+3H_(2)(g) hArr 2NH_(3)(g), DeltaH^(ɵ)=-22.4 kJ The pressure inside the chamber is 100 atm and temperature at 300 K The preparation of ammonia by Haber's process is an exothermic reaction. If the preparation follows the following temperature-pressure relationship for its % yield. Then for temperature T_(1), T_(2) and T_(3) the correct option is:
The potential associated. with each electrode is known as electrode potential. If the concentration of each species taking part in the electrode reaction is unity (if any gås appears in the electrode reaction, it is confined to 1 atmospheric pressure) and further the reaction is carried out at 298 K, then the potential of each electrode is said to be the standard electrode potential. By convention, the standard electrode potential of hydrogen electrode is 0:0 volt. The electrode potential value for each electrode process is a measure, of relative tendency of the active species in the process to remain in the oxidized / reduced form. A negative E^@ means that the redox couple is a stronger reducing agent than the H^(+)//H_2 couple. A positive E mears that the redox couple is a weaker reducing agent than. the H^(+)//H couple. The metal with greater positive value of standard reduction potentlal forms the oxide of greater thermal stability: Given the standard reduction potentials. E_(K^(+)//K)^(@)=-2.93V, E_(Ag^(+)//Ag)^(@)=+0.80V, E_(Hg^(+)//Hg)^(@)=0.79V E_(Mg^(+)//Mg)^(@)=-2.37V, E_(Cr^(3+)//Cr)^(@)=-0.74V The correct increasing order of reducing power is:
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Chemical reactions are invariably associated with the transfer of energy either in the form of hear or light. In the laboratory, heat changes in physical and chemical processes are measured with an instrument called calorimeter. Heat change in the process is calculated as: q= ms Delta T , s= Specific heat = c Delta T = Heat capacity. Heat of reaction at constant pressure is measured using simple or water calorimeter. Q_(v)= Delta U = Internal energy change, Q_(P) = DeltaH, Q_(P) = Q_(V) + P Delta V and DeltaH = Delta U+ Delta nRT . The amount of energy released during a chemical change depends on the physical state of reactants and products, the condition of pressure, temperature and volume at which the reaction is carried out. The variation of heat of reaction with temperature and pressure is given by Kirchoff's equation: (DeltaH_(2) - DeltaH_(1))/(T_(2)-T_(1))= Delta C_(P) (At constant pressure), (DeltaU_(2) - DeltaU_(1))/(T_(2)-T_(1)) = DeltaC_(V) (At constant volume) The enthalpy change (DeltaH) for the reaction N_(2) (g) + 3H_(2)(g) rarr 2NH_(3)(g) is -92.38kJ at 298 K. The internal energy change DeltaU at 298 K is
Compreshension -I The experimental values of colligative properties of many solutes in solution resembles calculated value of colligative properties. However in same cases, the experimental value of colligative property differ widely than those obtained by calculation. Such experimental values of colligative properties are known as Abnormal values of colligative properties are : (i) Dissociation of solute : It increases the colligative properties. (ii) Association of solute : It decreases the colligative properties e.g. : Dimerisation of acetic acid in benzene 4 different 100 ml solutions are prepared by mixing 1 gram each of NaCl (NH_(2))_(2)CO.Na_(2)SO_(4) and K_(4)[Fe(CN)_(6)] at temperature T. Correct order of osmotic pressure is
VMC MODULES ENGLISH-SURFACE CHEMISTRY-LEVEL-1
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