Question
Read the passage given below and answer the following questions: An ideal solution may be defined as the solution which obeys Raoult's law exactly over the entire range of concentration. The solutions for which vapour pressure is either higher or lower than that predicted by Raoult's law are called non-ideal solutions.Non-ideal solutions can show either positive or negative deviations from Raoult's law depending on whether the A-B interactions in solution are stronger or weaker than A - A and B - B interactions. The following questions are multiple choice questions. Choose the most appropriate answer:
  1. Which of the following solutions is/are ideal solution(s)?
  1. Bromoethane and iodoethane.
  2. Acetone and chloroform
  3. Benzene and acetone
  4. n-heptane and n-hexane
  1. Only I
  2. I and II
  3. II and III
  4. I and Iv
  1. For which of the following solutions $\Delta\text{H}_{\text{mix}}$ and $\Delta\text{V}_{\text{mix}}$ is negative?
  1. Acetone and aniline
  2. Ethyl alcohol and cyclohexane
  3. Acetone and CS2
  4. Benzene and toluene
  1. Which of the following is not true for positive deviations?
  1. The A-B interactions in solution are weaker than the A - A and B - B interactions.
  2. $\text{P}_\text{A}<\text{P}\mathring{\text{A}}\ \text{x}_\text{A}$ and $\text{P}_\text{B}<\text{P}\mathring{\text{B}}\ \text{x}_\text{B}$
  3. Carbon tetrachloride and chloroform mixture is an example of positive deviations.
  4. All of these.
  1. For water and nitric acid mixture, which of the given graph is correct?
 
  1.  
 
  1.  
  1. Both of these
  2. None of these
  1. Water-HCI mixture.
  1. Shows positive deviations.
  2. Forms minimum boiling azeotrope.
  3. Shows negative deviations.
  4. Forms maximum boiling azeotrope.
  1. I and II
  2. I and III
  3. I and IV
  4. III and IV

Answer

  1. (d) I and Iv
Explanation:
II represents negative deviations and III represents positive deviations.
  1. (a) Acetone and aniline
Explanation:
Acetone and aniline mixture represents negative deviations from Raoult's law, hence for this mixture,
$\Delta\text{H}_{\text{mix}}$ and $\Delta\text{V}_{\text{mix}}$ is negative.
  1. (b) $\text{P}_\text{A}<\text{P}\mathring{\text{A}}\ \text{x}_\text{A}$ and $\text{P}_\text{B}<\text{P}\mathring{\text{B}}\ \text{x}_\text{B}$
Explanation:
For positive deviations $\text{P}_\text{A}<\text{P}\mathring{\text{A}}\ \text{x}_\text{A}$ and $\text{P}_\text{B}<\text{P}\mathring{\text{B}}\ \text{x}_\text{B}$
  1. (b) 
Explanation:
Water and nitric acid mixture shows negative deviations from Raoult's law, hence 
 $\text{P}_\text{A}<\text{P}\mathring{\text{A}}\ \text{x}_\text{A}$ and $\text{P}_\text{B}<\text{P}\mathring{\text{B}}\ \text{x}_\text{B}$
  1. (d) III and IV
Explanation:
Water-HCI mixture shows negative deviations from Raoult's law and solutions showing negative deviations from ideal behaviour form maximum boiling azeotrope.

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Read the passage given below and answer the following questions:
Coordination compounds are formulated and named according to the $\text{IUPAC}$ system.
Few rules for naming coordination compounds are:
  1. In ionic complex, the cation is named first and then the anion.
  2. In the coordination entity, the ligands are named first and then the central metal ion.
  3. When more than one type of ligands are present, they are named in alphabetical order of preference without any consideration of charge.
The following questions are multiple choice questions. Choose the most appropriate answer:
  1. The $\ce{[Pt(NH_3)_3Br(NO_2)Cl]Cl}$ name of the complex $\ce{[Pt(NH_3)_3Br(NO_2)Cl]Cl}$ is:
  1. Triamminechlorobromonitroplatinum $(IV)$ chloride.
  2. Triamminebromonitrochloroplatinum $(IV)$ chloride.
  3. Triamminebromidochloridonitroplatinum $(IV)$ chloride.
  4. Triamminenitrochlorobromoplatinum $(IV)$ chloride.
  1. The $\text{IUPAC}$ name of $\ce{[Ni(CO)_4]}$ is:
  1. Tetracarbonylnickel $(II).$
  2. Tetracarbonylnickel $(0).$
  3. Tetracarbonylnickelate $(II).$
  4. Tetracarbonylnickelate $(0).$
  1. As per $\text{IUPAC}$ nomenclature, the name of the complex $\ce{[Co(H_2O)_4(NH_3)_2]Cl_3}$ is:
  1. Tetraaquadiamminecobalt $(II)$ chloride.
  2. Tetraaquadiamminecobalt $(III)$ chloride.
  3. Diamminetetraaquacobalt $(II)$ chloride.
  4. Diamminetetraaquacobalt $(III)$ chloride.
  1. Which of the following represents correct formula of dichloridobis $($ethane $-1, 2-$diamine$)$ cobalt $(III)$ ion?
  1. $\ce{[CoCl_2(en)]^{2+}}$
  2. $\ce{[CoCl_2(en)_2]^{2+}}$
  3. $\ce{[CoCl_2(en)]^+}$
  4. $\ce{[CoCl_2(en)_2]^+}$
  1. Correct formula of pentaamminenitro$-O-$cobalt $(III)$ sulphate is:
  1. $\ce{[Co(NO_2)(NH_3)_5]SO_4}$
  2. $\ce{[Co(ONO)(NH_3)_5]SO_4}$
  3. $\ce{[Co(NO_2)(NH_3)_4](SO_4)_2}$
  4. $\ce{[Co(ONO)(NH_3)_4](SO_4)_2}$
Read the passage given below and answer the following questions: Arrangement of ligands in order of their ability to cause splitting $(\Delta)$ is called spectrochemical series. Ligands which cause large splitting $($large $\Delta)$ are called strong field ligands while those which cause small splitting $($small $\Delta)$ are called weak field ligands. When strong field ligands approach metal atom/ ion, the value of $\Delta_0$ is large, so that electrons are forced to get paired up in lower energy $t_{2g}$ orbitals. Hence, a low$-$spin complex is resulted from strong field ligand. When weak field ligands approach metal atom/ ion, the value of $\Delta_0$ is small, so that electrons enter high energy egorbitals rather than pairing in low energy $t_{2g}$ orbitals. Hence, a high$-$spin complex is resulted from weak field ligands. Strong field ligands have tendency to form inner orbital complexes by forcing the electrons to pair up. Whereas weak field ligands have tendency to form outer orbital complex because inner electrons generally do not pair up. In these questions $(Q.$ No. $i-iv),$ a statement of assertion followed by a statement ofreason is given. Choose the correct answer out of the following choices.
  1. Assertion and reason both are correct statements and reason is correct explanation for assertion.
  2. Assertion and reason both are correct statements but reason is not correct explanation for assertion.
  3. Assertion is correct statement but reason is wrong statement.
  4. Assertion is wrong statement but reason is correct statement.
The following questions are multiple choice questions. Choose the most appropriate answer:
  1. Assertion: In tetrahedral coordination entity formation, the $d$ orbital splitting is inverted and is smaller as compared to the octahedral field splitting.
Reason : Spectrochemical series is based on the absorption of light by complexes with different ligands.
  1. Assertion: In high spin situation, configuration of $d^5$ ions will be $\text{t}^3_{2\text{g}}\text{e}^2_\text{g}.$
Reason : In high spin situation, pairing energy is less than crystal field energy.
  1. Assertion: $F^-$ ion is a weak field ligand and fonns outer orbital complex.
Reason : $F^-$ ion cannot force the electrons of $d_{z^2}$ and $d_{x^2-y^2}$ orbitals of the inner shell to occupy $d_{xy}, d_{yz}$ and $d_{zx} $orbitals of the same shell.
  1. Assertion: The crystal field model is successful in explaining the formation, structures, colour and magnetic properties of coordination compounds.
Reason: In spectrochemical series, ligands are arranged in a series of increasing field strength.
  1. Assertion: $NF_3$ is a weaker ligand than $N(CH_3)_3.$
Reason: $NF_3$ ionizes to give $F^-$ ions in aqueous solution.
Read the passage given below and answer the following questions:
A primary alkyl halide $(A) C_4H_9Br$ reacted with akoholic $\text{KOH}$ to give compound $(B).$ Compound $(B)$ is reacted with $\text{HBr}$ to give compound $(C)$ which is an isomer of $(A).$ When $(A)$ reacted with sodium metal, it gave a compound $(D) C_8H_{18}$ that is different than the compound obtained when n-butyl bromide reacted with sodium metal.
The following questions are multiple choice questions. Choose the most appropriate answer:
  1. Compound $(A)$ is:
  1. $\ce{CH_3CH_2CH_2CH_2Br}$
  2. $\text{CH}_3\text{CH}-\text{CH}_2\text{Br}\\\ \ \ \ \ \ \ \ \ |\\\ \ \ \ \ \ \ \ \text{CH}_3$
  3. $\ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{CH}_3\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\\text{CH}_3-\text{C}-\text{Br} \\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{CH}_3$
  4. $\ce{CH_3CH_2CH_2Br}$
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  1. Positional
  2. Functional
  3. Chain
  4. Both $(a)$ and $(c)$
  1. Identify compound $(B).$
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  2. $\ce{CH_3– CH = CH – CH_3}$
  3. $\ce{CH_3– CH_2 – CH = CH_2}$
  4. None of these.
  1. IUPAC name of compound $(D)$ is:
  1. $N -$ octane
  2. $2, 5 -$ dimethylhexane
  3. $2 -$ methylheptane
  4. $3, 4 -$ dimethyl hexane.
  1. When compoound $(C)$ is treated with ale. $\text{KOH}$ and then treated with presence of peroxide, the compound obtained is:
  1. $\ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{CH}_3\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\\text{CH}_3-\text{C}-\text{Br} \\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{CH}_3$
  2. $\ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{CH}_3\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\\text{CH}_3-\text{CH}-\text{CH}_2-\text{Br}$
  3. $\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{Br}$
  4. $\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}-\text{Br}\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{CH}_3$
For a first order reaction$, A \rightarrow$ Products$, \text{k}=\frac{2.303}{\text{t}}\log\frac{\text{a}}{\text{a}-\text{x}},$ where a is the initial concentration of $A$ and $(a - x)$ is the concentration of $A$ after time $t. k$ is rate constant. Its value is constant at constant temperature for a reaction. The time in which half of the reactant is consumed is called half$-$life period. Half$-$life period of a first order reaction is constant. Its value is independent of initial concentration or any other external conditions.In these questions $(Q.$ No. $i-iv),$ a statement of assertion followed by a statement ofreason is given. Choose the correct answer out of the following choices.
  1. Assertion and reason both are correct statements and reason is correct explanation for assertion.
  2. Assertion and reason both are correct statements but reason is not correct explanation for assertion.
  3. Assertion is correct statement but reason is wrong statement.
  4. Assertion is wrong statement but reason is correct statement.
  1. Assertion : Rate of reaction doubles when concentration of reactant is doubled if it is a first order reaction.
Reason : Rate constant also doubles.
  1. Assertion : For the first order reaction, half$-$life period is expressed as $\text{t}_\frac{1}{2}=\frac{2.303}{\text{k}}\log2.$
Reason : The half$-$life time of a first order reaction is not always constant and it depends upon the initial concentration of reactants.
  1. Reason : The half$-$life time of a first order reaction is not always constant and it depends upon the initial concentration of reactants.
Reason : Acid only acts as a catalyst whereas alkali acts as one of the reactants.
  1. Assertion : For a first order reaction, the concentration of the reactant decreases exponentially with time.
Reason : Rate of reaction at any time depends upon the concentration of the reactant at that time.
  1. Assertion : Half$-$life period for a first order reaction is independent of initial concentration of the reactant.
Reason : For a first order reaction, $\text{t}_\frac{1}{2}=\frac{0.693}{\text{k}},$ where $k$ is rate constant.
Read the passage given below and answer the following questions: Boiling point or freezing point of liquid solution would be affected by the dissolved solids in the liquid phase. A soluble solid in solution has the effect of raising its boiling point and depressing its freezing point. The addition of non-volatile substances to a solvent decreases the vapor pressure and the added solute particles affect the formation of pure solvent crystals. According to many researches the decrease in freezing point directly correlated to the concentration of solutes dissolved in the solvent. This phenomenon is expressed as freezing point depression and it is useful for several applications such as freeze concentration of liquid food and to find the molar mass of an unknown solute in the solution. Freeze concentration is a high quality liquid food concentration method where water is removed by forming ice crystals. This is done by cooling the liquid food below the freezing point of the solution. The freezing point depression is referred as a colligative property and it is proportional to the molar concentration of the solution (m), along with vapor pressure lowering, boiling point elevation, and osmotic pressure. These are physical characteristics of solutions that depend only on the identity of the solvent and the concentration of the solute. The characters are not depending on the solute’s identity.
  1. When a non volatile solid is added to pure water it will:
  1. boil above 100°C and freeze above 0°C
  2. boil below 100°C and freeze above 0°C
  3. boil above 100°C and freeze below 0°C
  4. boil below 100°C and freeze below 0°C
  1. Colligative properties are:
  1. dependent only on the concentration of the solute and independent of the solvent’s and solute’s identity.
  2. dependent only on the identity of the solute and the concentration of the solute and independent of the solvent's identity.
  3. dependent on the identity of the solvent and solute and thus on the concentration of the solute.
  4. dependent only on the identity of the solvent and the concentration of the solute and independent of the solute’s identity.
  1. Assume three samples of juices A, B and C have glucose as the only sugar present in them. The concentration of sample A, B and C are 0.1M, 5M and 0.2 M respectively. Freezing point will be highest for the fruit juice:
  1. A
  2. B
  3. C
  4. All have same freezing point
  1. Identify which of the following is a colligative property:
  1. freezing point
  2. boiling point
  3. osmotic pressure
  4. all of the above
Read the passage given below and answer the following questions:
Amines are basic in nature. The basic strength of amines can be expressed by their dissociation constant, $K_b$ or $pK_b.$
$\text{RNH}_2+\text{H}_2\text{O}\rightleftharpoons\text{RNH}^+_3+\text{OH}^-$
$\text{k}_\text{b}=\frac{[\text{RNH}^+_3][\text{OH}^-]}{[\text{RNH}_2]}\text{and}\text{ pk}_\text{b}=-\log\text{k}_\text{b}$
Greater the $K_b$ value or smaller the $pK_b$ value, more is the basic strength of a mine. Aryl amines such as aniline are less basic than aliphatic amines due to the involvement of lone pair of electrons on $N-$atom with the resonance in benzene. In derivatives of aniline, the electron releasing groups increase the basic strength while electron withdrawing groups decrease the basic strength. The base weakening effect of electron withdrawing group and base strengthening effect of electron releasing group is more marked at $p-$position than at $m-$position. $a-$Substituted aniline is less basic than aniline due to ortho effect and is probable due to combination of electronic and steric effect.
The following questions are multiple choice questions. Choose the most appropriate answer:
  1. Which of the following has lowest $pK_b$ value?
  1. The strongest base among the following is:
  1. $\ce{C_6H_5NH_2}$
  2. $\ce{p-NO_2 - C_6H_4NH_2}$
  3. $\ce{m-NO_2 - C_6H_4NH_2}$
  4. $\ce{C_6H_5CH_2NH_2}$
  1. Maximum $pK_b$ value of:
  1.  
  1.  
  1. $\ce{(CH_3CH_2)_2NH}$
  2. $\ce{(CH_3)_2NH}$
  1.  The order of basic strength among the following amines in benzene solution is:
  1. Methylamine is more basic than $NH_3.$
  2. Amines form hydrogen bonds.
  3. Ethylamine has higher boiling point than propane.
  4. Dimethylamine is less basic than methylamine.
  1. $\ce{CH_3CH_2NH_2}$ contains a basic $-NH_2$ group, but $\ce{CH_3CONH_2}$ does not because:
  1. Acetamide is amphoteric in character.
  2. In ethylamine the electron pair on $N-$atom is delocalised by resonance.
  3. In ethylamine there is no resonance while in acetamide the lone pair of electrons on $N-$ atom is delocalised and is less available for protonation.
  4. None of these.
Read the passage given below and answer the following questions:
The concentration of a solute is very important in studying chemical reactions because it determines how often molecules collide in solution and thus indirectly determine the rate of reactions and the conditions at equilibrium. There are several ways to express the amount of solute present in a solution. The concentration of a solution is a measure of the amount of solute that has been dissolved in a given amount of solvent or solution. Concentration can be expressed in terms of molarity, molality, parts per million, mass percentage, volume percentage, etc.
The following questions are multiple choice questions. Choose the most appropriate answer:
  1. A solution is prepared using aqueous $Kl$ which is turned out to be $20\%$ w/w Density of $Kl$ is $1.202 g/mL$ the molality of the given solution and mole fraction of solute are respectively.
  1. $1.95m, 0.120$
  2. $1.5m, 0.0263$
  3. $2.5m, 0.0569$
  4. $3.0m, 0.0352$
  1. The molarity $($in mol $L^{-1})$ of the given solution will be.
  1. $1.56$
  2. $1.89$
  3. $0.263$
  4. $1.44$
  1. Which of the following is correct relationship between mole fraction and molality?
  1. $\text{x}_2=\frac{\text{mM}_1}{1+\text{mM}_1}$
  2. $\text{x}_2=\frac{\text{mM}_1}{1-\text{mM}_1}$
  3. $\text{x}_2=\frac{1+\text{mM}_1}{\text{mM}_1}$
  4. $\text{x}_2=\frac{1-\text{mM}_1}{\text{mM}_1}$
  1. Which of the following is temperature dependent?
  1. Molarity
  2. Molality
  3. Mole fraction
  4. Mass percentage
  1. Which of the following is true for an aqueous solution of the solute in terms of concentration?
  1. $1M = 1m$
  2. $1M > 1m$
  3. $1M < 1m$
  4. Cannot be predicted
Read the passage given below and answer the following questions:
Both alcohols and phenols are acidic in nature, but phenols are more acidic than alcohols. Acidic strength of alcohols mainly depends upon the inductive effect. Acidic strength of phenols depends upon a combination of both inductive effect and resonance effects of the substituent and its position on the benzene ring. Electron withdrawing groups increases the acidic strength of phenols whereas electron donating groups decreases the acidic strength of phenols. Phenol is a weaker acid than carboxylic acid.
The following questions are multiple choice questions. Choose the most appropriate answer:
  1. Phenols are highly acidic as compare to alcohols due to:
  1. The higher molecular mass of phenols.
  2. The stronger hydrogen bonds in phenols.
  3. Alkoxide ion is a strong conjugate base.
  4. Phenoxide ion is resonance stabilised.
  1. The correct order of acidic strength among the following is:
  1. $(III) > (IV) > (II) > (I)$
  2. $(IV) > (III) > (I) > (II)$
  3. $(IV) > (III) > (II) > (I)$
  4. $(I) > (II) > (IV) > (III)$
  1. The correct decreasing order of $pK_a$ value is:
  1. $II > IV > I > III$
  2. $IV > II > III > I$
  3. $II I> II > IV > I$
  4. $IV > I > II > III$
  1. The compound that does not liberate $CO_2,$ on treatment with aqueous sodium bicarbonate solution is:
  1. Benzoic acid.
  2. Benzenesulphonic acid.
  3. Salicylic acid.
  4. Carbolic acid.
  1. Most acidic amongst the following is:
Read the passage given below and answer the following questions: Werner, a Swiss chemist in $1892$ prepared and characterised a large number of coordination compounds and studied their physical and chemical behaviour. He proposed that, in coordination compounds, metals possess two types of valencies, viz. primary valencies, which are normally ionisable and secondary valencies which are non $-$ ionisable. ln a series of compounds of cobalt $(III)$ chloride with ammonia, it was found that some of the chloride ions could be precipitated as $\text{AgCl}$ on adding excess of $\ce{AgNO_3}$ solution in cold, but some remained in solution. The number ofions furnished by a complex in a solution can be determined by precipitation reactions. The measurement of molar conductance of solutions of coordination compounds helps to estimate the number of ions furnished by the compound in solution. In these questions $(Q$. No. $i-iv),$ a statement of assertion followed by a statement ofreason is given. Choose the correct answer out of the following choices.
  1. Assertion and reason both are correct statements and reason is correct explanation for assertion.
  2. Assertion and reason both are correct statements but reason is not correct explanation for assertion.
  3. Assertion is correct statement but reason is wrong statement.
  4. Assertion is wrong statement but reason is correct statement.
The following questions are multiple choice questions. Choose the most appropriate answer:
  1. Assertion : The complex $[\ce{Co(NH_3)_3Cl_3]}$ does not give precipitate with silver nitrate solution.
Reason : The given complex is non-ionisable.
  1. Assertion : The complex $\ce{[Co(NH_3)_4Cl_2]Cl}$ gives precipitate corresponding to $2$ mol of $\ce{AgCl}$ with $\ce{AgNO_3}$ solution.
Reason : It ionises as $\ce{[Co(NH_3)_4Cl_2]^+ + Cl}^-.$
  1. Assertion : $\ce{CoCl_3. 4NH_3}$ gives $1$ mol of $\ce{AgCl}$ on reacting with $\ce{AgNO_3},$ its secondary valency is $6$.
Reason : Secondary valency corresponds to coordination number.
  1. Assertion : $1$ mol of $\ce{[CrCl_2(H_2O)_4]Cl· 2H_2O}$ will give $1$ mol of $\ce{AgCl}$ on treating with $\ce{AgNO_3}.$
Reason : $ Cl^-$ ions satisfying secondary valanceis will not be precipitated.
  1. Assertion : $\ce{CoCl_3. 3NH_3}$ is not conducting while $\ce{CoCl_3. 5NH_3}$ is conducting.
Reason : The complex of $\ce{CoCl_3. 3NH_{3 }}$ is $\ce{[CoCl_3(NH_3)_3]}$ while that of $\ce{CoCl_3· 5NH_3}$ is $\ce{[CoCl(NH_3)_5]Cl_3}.$
Read the passage given below and answer the following questions:
The aryl halides are relatively less reactive towards nucleophilic substitution reactions as compared to alkyl halides. This low reactivity can be attributed to the following factors:
  • The $C - X$ bond in halobenzene has a partial double bond character due to involvement of halogen electrons in resonance with benzene ring.
  • The $C - X$ bond in aryl halides is less polar as compared to that in alkyl halides as $sp^2$ hyridised carbon is more electronegative than $sp^3$ hybridised carbon.
In these questions $(Q. No. i-Iv),$ a statement of assertion followed by a statement of reason is given. Choose the correct answer out of the following choices.
  1. Assertion and reason both are correct statements and reason is correct explanation for assertion.
  2. Assertion and reason both are correct statements but reason is not correct explanation for assertion.
  3. Assertion is correct statement but reason is wrong statement.
  4. Assertion is wrong statement but reason is correct statement.
  1. Assertion: Primary benzylic halides are more reactive than primary alkyl halides towards $S_N1$ reactions.
Reason: Reactivity depends upon the nature of the nucleophile and the solvent.
  1. Assertion: is more reactive than towards nucleophilic substitution reactions.
Reason: Tertiary alkyl halides react predominantly by $S_N1$ mechanism.
  1. Assertion: Chlorobenzene is more reactive than $p-$chloroanisole to nucleophilic substitution reactions.
Reason: Greater the stability of carbanion, greater is its ease of formation and hence, more reactive is the aryl halide.
  1. Assertion: $4-$Nitrochlorobenzene undergoes nucleophilic substitution more readily than chlorobenzene.
Reason: Chlorobenzene undergoes nucleophilic substitution by elimination-addition mechanism while $4-$nitrochlorobenzene undergoes nucleophilic substitution by addition$-$elimination mechanism.
  1. Assertion: Chlorobenzene is less reactive than benzene towards the electrophilic substitution reaction.
Reason: Resonance destabilises the carbocation.