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2401.

Which of the following liberate hydrogen on reaction with dilute `H_(2)SO_(4)`A. FeB. CuC. AlD. Hg

Answer» Correct Answer - C
`2Al+dil.H_(2)SO_(4)toAl_(2)SO_(4)+H_(2)uarr`.
2402.

For a reaction `A(s)+2B^(o+) rarr A^(2+)+2B` `K_(c)` has been found to be `10^(12)`. The `E^(c-)._(cell)` isA. `0.354V`B. `0.708V`C. `0.0098V`D. `1.36V`

Answer» Correct Answer - a
`E=E^(c-)-(0.059)/(2) log K`
At equilibrium, `E=0`
`E^(c-)=(0.059)/(2) log K =(0.059)/(2) log 10^(12)`
`=(0.059)/(2)xx12=0.354`
2403.

Zinc can be coated on iron to produce galvanised iron but the reverse is not possible. It is becauseA. zinc is lighter than ironB. zinc has lower melting point than ironC. zinc has lower negative electrode potential than ironD. zinc has higher negative electrode potential than iron

Answer» Correct Answer - D
Zinc has higher negative electrode potential than iron, so iron cannot be coated on zinc.
2404.

Galvanized iron sheets are coated withA. CopperB. NickelC. ZincD. Carbon

Answer» Correct Answer - c
Factual statement
2405.

Galvanized iron sheets and coated withA. NickelB. ChromiumC. CopperD. Zinc.

Answer» Correct Answer - D
G.I. sheets are coated with zinc .
2406.

Galvanized iron sheets are coated withA. `Cr`B. `Zn`C. `Ni`D. `Cu`

Answer» Correct Answer - B
Galvanized iron is sheet iron coated with a layer of `Zn` to prevent corrosion, usually made by dipping the sheet `Al` added to prevent the formation of a brittle `Zn-Fe` alloy, Thus, galvanized iron is sometimes called Zinc-plated iron. Zinc is more easily oxidized than iron:
`Zn(s) rarr Zn^(2+)(aq.)+2e^(-) E^(@) = +0.76V`
So even if a scratch exposes the iron, the `Zn` is still attacked In this case, the `Zn` metal scrves as the anode and the iron is the cathode.
2407.

Three ions sheets have been coated separately with three metals (A,B and C) whose standard electrode potentials are given below: `{:("Metal",A,B,C,"Iron"),(E_("value")^(@),-0.46,-0.66V,-0.20V,-0.44V):}` Identify in which case rusting will take place faster when coating is damaged.

Answer» Comparing oxidation potential of iron with those of metals A,B and C, iron has higher oxidation potential than C only. Hence, when coating of C is broken, rusting will become faster.
2408.

There iron sheets have been coated separately with three metals (A,B and C ) whose standard electrode potentials are given below. `{:("Metal"," "A," "B," "C," "Iron),(,-0.46" V",-0.66" V",-0.20" V",-0.44" V"):}` Identify in which case rusting will take place faster when coating is damaged.

Answer» Rusting of iron will occur faster when coated with metal C because it is placed above iron in the activity series. Iron will take part in redox reaction and not the metal C.
2409.

`E^(@)` of `Mg^(2+) || Mg, Zn^(2+) || Zn`, and `Fe^(2+)||Fe` are -2.37V, -0.76V and -0.44 V respectively. Which of the following is correct?A. Mg oxidises FeB. Zn oxidises `Fe`C. Zn reduces `Mg^(2+)`D. Zn reduces `Fe^(2+)`

Answer» Correct Answer - D
`E_(op(Zn))^(@) gt E_(op(Fe))^(@)`
Thus `Zn to Zn^(2+) + 2e`
and `Fe^(2+)+ 2e to Fe`
2410.

For how long 2.5 ampere of current is passed to supply 5400C of charge?A. 1hrB. 2.5hrC. 6hrD. 9 hr.

Answer» Correct Answer - C
`Q=1t`
`t=(Q)/(I)=(54000)/(2.5"amp")=(21600)/(60xx60)` hours
= 6 hours.
2411.

How many coulombs of electricity are required for complete oxidation of 90 g of `H_(2)O`?

Answer» 90g of `H_(2)O=(90)/(18)" moles"=5"moles"`
1 mole of `H_(2)O` requires electricity=2F
`therefore`5moles of `H_(2)O` will require electricity`=5xx2F=10F=10xx96500=965000C`
(ii) 1000 mL of 1 M `KMnO_(4)` solution contain `KMnO_(4)=1` mol
`therefore`100 mL of 0.1 M `KMnO_(4)` solution contain `KMnO_(4)=(1)/(1000)xx100xx0*1mol=0*01`mol
1 mole of `KMnO_(4)` requires electricity=5F
`therefore0*01" mol of "KMnO_(4)` will require electricity=`0*01xx5F=0*05F=0*05xx96500C=4825C`
2412.

How much charge is required for the following reaction? (i) 1mol of `Al^(3+)` to Al. (ii) 1 mol of `Cu^(2+)` to Cu. (iii) 10 mole of `MnO_(4)^(-)` to `Mn^(2+)`

Answer» (i) The electrode reaction is: `Al^(3+)+3e^(-)toAl`
`therefore` Quantity of charge required for reduction of 1 mole of `Al^(3+)=3F=3xx96500C=289500C`.
(ii) The electrode reaction is: `Cu^(2+)+2e^(-)toCu`
`therefore`Quantity of charge required for reduction of 1 mol of `Cu^(2+)=2` faradays`=2xx96500C=193000C` ltBrgt (iii) The electrode reaction is `MnO_(4)^(-)toMn^(2+)`, i.e., `Mn^(7+)5e^(-)toMn^(2+)`
`therefore`Quantity of charge required `=5F=5xx96500C=482500C`.
2413.

A current of 2.6 ampere was passed through `CuSO_(4)` solution for 380 sec . The amount of Cu deposited is (atomic mass of Cu 63.5)A. `0.3250 g`B. `0.635` gC. `6.35` gD. `3.175 g`

Answer» Correct Answer - A
`W = (E xxi xx t)/(96500) = (63.5 xx 2 .6 xx380)/(2 xx 96500) = 0.325` g
2414.

How many coulombs are required for the oxidation of `1 mol` of `H_(2)O` to `O_(2)`?A. `9.65xx10^(4)C`B. `4.825xx10^(5)C`C. `1.93xx10^(5)C`D. `1.93xx10^(4)C`

Answer» Correct Answer - C
`H_(2)Orarr1//2O_(2)+2H^(+)+2e^(-)`
1 mole 2 mole(2F)
`=2xx96500C`
`=1.93xx10^(5)C`
2415.

How many coulombs are required for the oxidation of 1 mol of `H_(2)O_(2)` ?A. `9.65 xx 10^(4) C`B. `93000 C`C. `1.93 xx 10^(5) C`D. `19.3 xx 10^(2) C`

Answer» Correct Answer - C
`H_(2) O_(2) rarr O_(2) + 2H^(+) + 2e^(-)`
1 mol `H_(2) O_(2) -= 2 mol e^(-)`
`-= 2 xx 96500 C`
`= 1.93 xx 10^(5) C`
2416.

The charge in coulombs on 1 g ion of `N^(3-)` isA. 96500B. `2.89xx10^(5)`C. `1.45xx10^(6)`D. `6xx10^(23)`

Answer» Correct Answer - B
One `N^(3-)` ion has 3 units of electric charge
`therefore` 1 g ion of `N^(3-)` has `3xx6.023xx10^(23)` electrons
or 1 g ion of `N^(3-)` has `3xx6.023xx10^(23)` electrons
or 1 g ion `N^(3-)` has `3xx96500` coulomb charge
`=289500=2.89xx10^(6)C`
2417.

How many atoms of hydrogen are liberated at cathode , when 965 coulombs of charge is passed through water ?A. `6.02 xx 10^(21)`B. `6.02 xx 10^(23)`C. `6.02 xx 10^(-19)`D. `6.02 xx 10^(19)`

Answer» Correct Answer - A
`H_(2)O to H_(2) + (1)/(2) O_(2) or 2 H^(+) + 2e^(-) to 2H` i.e., 96500 C produce 1 mole H-atoms = `6.02 xx 10^(23)` atoms . So 965 C will produce H-atoms = `6.02 xx 10^(21)`.
2418.

Calculate the charge in coulombs required for the oxidation of: (i) 2 moles of `H_(2)O` to `O_(2)`

Answer» (i) The electrode reaction for 1 mole of `H_(2)O` is:
`H_(2)O to H_(2)+(1)/(2)O_(2), i.e., O^(2-) to (1)/(2)O_(2)+2e^(-)` or `2H^(+)+2e^(-)toH_(2)`
or `H_(2)Oto2H^(+)+(1)/(2)O_(2)+2e^(-)`
`therefore` Quantity of electricity required for oxidation of 1 mol of `H_(2)O=2F`
or Quantity of electricity required for oxidation of 2 moles of `H_(2)=4F=4xx96500C=386000C`
(ii) The electrode reaction for 1 mole of FeO is: `FeOto(1)/(2)Fe_(2)O_(3), i.e., Fe^(2+) to Fe^(3+)+e^(-)`
`therefore` Quantity of electricity required`=1F=96500C`.
2419.

When a current of 0.75 A is passed through `CuSO_(4)` solution of 25 min, 0.369g of copper is deposited at the cathode. Calculate the atomic mass of copper.

Answer» Quantity of electricity passed `=(0.75A)(25xx60s)=1125C`
`Cu^(2+) to 2e^(-)toCu`
Thus, 1 mole of Cu (i.e., gram atomic mass) is deposited by 2F, i.e, `2xx96500C`
Now, `1125` C deposit Cu=0.369 g
`2xx96500C` will deposit Cu=`(0.369)/(1125)xx2xx96500g=63.3g`
hence, atomic mass of copper=63.3
2420.

Statement : At the end of electrolysis using platinum electrodes, an aqueous solution of copper sulphate turn colourless. Explanation : Copper in copper sulphate is converted to copper hydroxide during the electrolysis.A. `S` is correct but `E` is wrongB. `S` is wrong but `E` is correct.C. Both `S` and `E` are correct and `E` is correct explanation of `S`.D. Both `S` and `E` are correct but `E` is not correct explanation of `S`.

Answer» Correct Answer - A
During electrolysis `CuSO_(4)` converted into `Cu`.
2421.

Calculate the quantity of electricity that would be required to reduce 12.3g of nitrobenzene to aniline, if the current efficiency for the process is 50%. If the potential drop across the cell is 3.0V, how much energy will be consumed?

Answer» Correct Answer - 347.40kJ
2422.

Resistance of ` 0.2 M` solution of an electrolue is ` 50 Omega`. The specific conductance of the solution is ` 1.4 S m^^(-1)`. The resistance of `0.5` M solution of the same electrolyte is `280. Omega`. The molar conducitivity of ` 0.5 M` solution of the electrolyte is ` S m^2 "mol"^(-1)` is.A. ` 5 xx10^(-4)`B. `5 xx10^(-3)`C. `5 xx10^3`D. `5 xx10^2`

Answer» Correct Answer - A
For `0.2 M` solution , ` R= 50 Omega`
` k= 14 S m^(-1) = 1.4 xx 10^(-2) S cm^(-1)`
The resistivity of the solution is related to specific cnductance by
` rho = 1/k = 1/(1.4 xx 10^(-2)) Omega cm`
It is known that , `R= rho 1/a`
It is kinown tht , `R= rho = 1/a`
`rArr l/a = R xx 1/(rho) = 50 xx 1.4 xx 10^(-2) cm`
for `0.5 M` solution,
`R= 280 Omega`
` k=? `
`l/a = 50 xx 1.4 xx 10^(-2) xm`
The specific conductance of the solution is given by
` k= 1/(rho) = 1/R xx l/a`
` k= 1/(280) xx 50 xx 1.4 xx 10^(-2)`
`2.5 xx 10^(-3) S cm^(-1)`
Now , the molar conductivity of the solution is given by
`Lambda_m = (K xx 1000)/M = (2.5 xx 10^(-3) xx 1000)/(0.5)`
` 5.5 cm^2 "mol"^(-1)`
` = 5 xx 10^(-4) S m^2 "mol"^(-1)`
Hence, the molar conductivity of `0.5 M` solution of the electrolyte is `5xx 10^(-4) Sm^2 "mol"^(-1)`.
2423.

The molar conducatance of `Ba^(2+)` and `Cl^(-)` are `127` and `76 ohm^(-1) cm^(-1) mol^(-1)` respectively at infinite dilution. The equivalent conductance of `BaCl_(2)` at infinte dilution will beA. 101.5B. 139.5C. 203.5D. 279.5

Answer» Correct Answer - B
`lamda^(oo)BaCl_(2)=(1)/(2)lamda^(oo)Ba^(2+)+lamda^(oo)Cl^(-)`
`=(127)/(2)+76=139.5ohm^(-1)cm^(-1)eq^(-1)`.
2424.

How many atoms of calcium will be deposited from a solution of `CaCl_(2)` by a current of 5mA flowig for 60s?A. `4.68xx10^18`B. `4.68xx10^15`C. `4.68xx 10^12`D. `4.68xx10^9`

Answer» Correct Answer - A
Quantity of electricity passed`=(25)/(1000)xx60=1.5`
`2F=2xx96500C` deposit `Ca=`1mole
`therefore1.5`C will deposit Ca=1mole
`therefore1.5C` will deposit `Ca=(1)/(2xx96500)xx1.5`mole
`=(1)/(2xx96500)xx1.5xx6.023xx10^(23)`atom`=4.68xx10^(18)`
2425.

The molar conducatance of `Ba^(2+)` and `Cl^(-)` are `127` and `76 ohm^(-1) cm^(-1) mol^(-1)` respectively at infinite dilution. The equivalent conductance of `BaCl_(2)` at infinte dilution will beA. `139.5"ohm"^(-1) "cm"^(2) "eq"^(-1)`B. `203"ohm"^(-1) "cm"^(2) "eq"^(-1)`C. `279"ohm"^(-1) "cm"^(2) "eq"^(-1)`D. `101.5"ohm"^(-1) "cm"^(2) "eq"^(-1)`

Answer» Correct Answer - A
`BaCl_2 to Ba^(2+) + 2Cl^(-)`
`Lambda_(BaCl_2)^@ = Lambda_(Ba^(2+))^@ + 2Lambda_(Cl^-)^@`=127 + ( 2 x 76 )
`279 "ohm"^(-1) "cm"^(2) eq^(-1)`
Equivalent conductivity =`279/2`=139.5 `"ohm"^(-1) "cm"^(2) eq^(-1)`
2426.

The molar conducatance of `Ba^(2+)` and `Cl^(-)` are `127` and `76 ohm^(-1) cm^(-1) mol^(-1)` respectively at infinite dilution. The equivalent conductance of `BaCl_(2)` at infinte dilution will beA. 139.52B. 203C. 279D. 101.5

Answer» Correct Answer - A
(a)The equivalent conductance of `BaCl_(2)` at infinite dilution.
`lambda_(oo) " of " BaCl_(2)=(1)/(2) lambda_(oo) " of " Ba^(2+) + lambda_(oo) " of " Cl^(-)`
`=(127)/(2)+76=139.5`
2427.

The molar conducatance of `Ba^(2+)` and `Cl^(-)` are `127` and `76 ohm^(-1) cm^(-1) mol^(-1)` respectively at infinite dilution. The equivalent conductance of `BaCl_(2)` at infinte dilution will beA. `330 Omega^(-1) cm^(2)`B. `203 Omega^(-1) cm^(2)`C. `139.5 Omega^(-1) cm^(2)`D. `51 Omega^(-1) cm^(2)`

Answer» Correct Answer - C
`Lambda_(m)^(oo)` for `BaCl_(2)=Lambda_(m)^(oo) Ba^(2+)+2Lambda_(m)^(oo)Cl^(-)`
`:. Lambda_(eq)^(oo)` for `BaCl_(2)=1/2 Lambda_(m)^(oo)Ba^(2+)+Lambda_(m)^(oo)Cl^(-)`
`=1/2 xx127+76=139.5 Omega^(-1) cm^(2)`
2428.

The molar conducatance of `Ba^(2+)` and `Cl^(-)` are `127` and `76 ohm^(-1) cm^(-1) mol^(-1)` respectively at infinite dilution. The equivalent conductance of `BaCl_(2)` at infinte dilution will beA. `139.52`B. `203`C. `279`D. `101.5`

Answer» Correct Answer - A
According to Kohlrausch law of independent migration of ions, limiting equivalent conductance of an electrolyte can be represented as the sum of the individual contributions of the anion and cation of the electrolyte, Thus
`Lambda_(eq.)^(@)(BaCl_(2))=lamda_(eq.)^(@)(Ba^(2+))+lamda_(eq.)^(@)(Cl^(-))`
Since `Ba^(+)` is divalent while `Cl^(-)` is univalent, `lamda_(eq.)^(@)(Ba^(2+)) = 1//2`
`lamda_(m)^(@)(Ba^(2+)` while `lamda_(eq.)^(@)(Cl^(-)) = lamda_(m)^(@)(Cl^(-))`. Thus
`lamda_(eq.)^(@)(BaCl^(2)) = ((127)/(2)+76) ohm^(-1) cm^(-1) eq^(-1)`
`=139.5 ohm^(-1) cm^(-1) eq^(-1)`
2429.

The equilibrium constant (K) for the reaction `Cu(s)+2Ag^(+) (aq) rarr Cu^(2+) (aq)+2Ag(s)`, will be [Given, `E_(cell)^(@)=0.46 V`]A. `K_(C) = AL (15.6)`B. `K_(C) = AL(2.5)`C. `K_(C) = AL (1.5)`D. `K_(C) = AL (12.2)`

Answer» Correct Answer - A
`E^(@) = (0.0592)/(n) "log" K_(C)`
`therefore log K_(C) = (E^(@) xx n)/(0.0592) = (0.46 xx 2 )/(0.0592) = 15.6`
`therefore K_(C) = AL (15.6)`
2430.

The emf of the cell, `Pt|H_(2)(1atm)|H^(+) (0.1M, 30mL)||Ag^(+) (0.8M)Ag` is `0.9V`. Calculate the emf when `40mL` of `0.05M NaOH` is added.

Answer» Correct Answer - `0.95V`
`E = E^(@) - 0.0591 log.([H^(+)])/([Ag^(+)])`
`0.9 - E^(@) - 0.0591 log.(0.1)/(0.8)`
`E^(@) = 0.84662`
On adding `40mL` of `0.05M NaOH`
`(0.05M NaOH 40 mL)` ltbr. `[H^(+)] = (3-2)/(70) = (1)/(70)`
now
`E = E^(@) - 0.0591 log.([H^(+)])/([Ag^(+)])`
`E = 0.84662 - 0.0591 log.(1)/(70 xx 0.8)`
`E = 0.95V`
2431.

The standard reduction potential for `Fe^(2+)//Fe and Sn^(2+)//Sn` electrode are -0.44 and -0.14 volt respectively. For the givencell reaction `Fe^(2+)+SntoFe+Sn^(2+)`, the standard EMF is:-A. `+0.30V`B. `-0.58V`C. `+0.58V`D. `-0.30V`

Answer» Correct Answer - D
For the cell reaction, Fe acts as cathode as Sn as anode. Hence,
`E_(cell)^(o)=E_(cathode)^(o)-E_("anode")^(o)=-0.44-(-0.14)=-0.30V`
the negative EMF suggests that the reaction goes spontaneously in reverse direction.
2432.

The standard reduction potential for `Fe^(2+) //Fe` and `Sn^(2+) //Sn` electrodes are `-0.44` and `-0.14 ` volt respectively. For the given cell reaction `Fe^(2+) + Sn rarr Fe + Sn^(2+) `, the standard ` EMF` is.A. ` +.030 V`B. `-0.58 V`C. ` +0. 58 V`D. ` -0. 30 V`

Answer» Correct Answer - D
For the cell reaction. Fe acts as cathode and Sn as anode, Hence,
`E_(cell)^2 -E_("cathode")^2 -E_("anode")^@ =- 0.44-(-0.14) =- 0.30 V`
The negative EMF suggests that the reaction goes spontaneously in reversed direction.
2433.

The standard reduction potential for `Fe^(2+) //Fe` and `Sn^(2+) //Sn` electrodes are `-0.44` and `-0.14 ` volt respectively. For the given cell reaction `Fe^(2+) + Sn rarr Fe + Sn^(2+) `, the standard ` EMF` is.A. `+.030v`B. `-0.58v`C. `+0.58v`D. `-0.300`

Answer» Correct Answer - D
The two half cell reactions are
`SnrarrSn^(2+)+2e^ (-)`
`Fe^(2+)+2e^(-)rarrFe`
`therefore` cell representation is
`Sn|Sn^(2+)||Fe^(2+)|Fe`
`E_("cell")^(@)=E_(Fe^(2+)//Fe)^(@)-E_(Sn^(2+)//Sn)^(@)`
`=-0.44V-(-0.14V)=0.30V`
2434.

The standard reduction potential for `Fe^(2+) //Fe` and `Sn^(2+) //Sn` electrodes are `-0.44` and `-0.14 ` volt respectively. For the given cell reaction `Fe^(2+) + Sn rarr Fe + Sn^(2+) `, the standard ` EMF` is.A. ` -0 . 30 V`B. ` -0 . 58 V`C. ` +0. 58 V`D. ` + 0. 3 0 V`

Answer» Correct Answer - A
For the cell reaction.Fe acts as cathode and Sn as anode, Hence,
`E_("cell")^2 -E_("cathode")^2 -E_("anode")^@ =- 0.44-(-0.14) =- 0.30 V`
The negative EMF suggests that the reaction goes spontaneously in reversed direction.
2435.

Given, standard electrode potentials `Fe^(2+) +2e^(-) rarr Fe, E^(@)=-0.440 V` `Fe^(3+)+3e^(-) rarr Fe, E^(@)=- 0.036 V` The standarde potential `(E^(@))` for `Fe^(2+)+e^(-) rarr Fe^(2+)`, isA. `+0.772 V`B. `-0.772 V`C. `+0.417 V`D. `-0.417 V`

Answer» Correct Answer - A
`Fe^(2+)+2e^(-) rarr Fe, DeltaG^(@)=-nFE^(@)` …(i)
`DeltaG^(@)=-2xxFxx(-0.440V)=0.880 F`
`Fe^(3+)+3e^(-) rarr Fe` …(ii)
`DeltaG^(@)=-3xxFxx(-0.036)`
`=0.108 F`
On subtracting Eq. (ii) from Eq. (i) we get
`Fe^(3+) +e^(-) rarr Fe^(2+)`
`DeltaG^(@)=0.108 F-0.880 F=-0.772 F`
`E^(@)=(-DeltaG^(@))/(nF)=((-0.772 F))/(1xxF)= +0.772 V`
2436.

Given standard `E^(c-):` `Fe^(3+)+3e^(-)rarrFe," "E^(c-)=-0.036` Fe^(2+)+2e^(-)rarr Fe," "E^(c-)=-0.440V` The `E^(c-)` of `Fe^(3+)+e^(-) rarr Fe^(2+) ` isA. `-0.476V`B. `-0.404V`C. `0.404V`D. `0.772V`

Answer» Correct Answer - d
`Fe^(3+)+3e^(-) rarr Fe(E_(1))" "(i)`
`Fe^(2+)+2e^(-) rarr Fe(E_(2))" "(ii)`
Net equation
`Fe^(3+)+e^(-) rarr Fe^(2+)(E_(3))" "(iii)`
`[` Obtained by `Eqs. (i)-(ii)]`
`E_(3)=(n_(1)E_(1)-N_(2)e_(2))/(n_(3))=(3(-0.036)-2(-0.0440))/(1)`
`=0.772V`
2437.

The standard reduction for the following reactions are : `Fe^(3+) + 3e^(-) rarr Fe` with `E^(@) = - 0.036 V` `Fe^(2+) + 2e^(-) rarr Fe` with `E^(@) = - 0.44 V` What would be the standard electrode potential for the reaction `Fe^(3+) + e^(-) rarr Fe^(2+)` ?A. 0.772 VB. 0.077 VC. `-0.404 V`D. `0.772 V`

Answer» Correct Answer - A
`{:(Fe^(3+)+3e^(-) rarr Fe,E_(1)^(@)=-0.036 V" "(n_(1)=3)),(Fe" "rarr Fe^(2+)+2e^(-),E_(2)^(@)=+0.44 V" "(n_(2)=2)),(bar(Fe^(3+)+e^(-) rarr Fe^(2+)" "),E_(3)^(@)=?" "(n_(3)=1)):}`
`n_(3)E_(3)^(@)=n_(1)E_(1)^(@)+n_(2)E_(2)^(@)`
`1xxE_(3)^(@)=3(-0.036)+2(+0.44)`
`E_(3)^(@)=0.772 V`
2438.

A hydrogen electrode X was placed in a buffer solution of sodium acetate and acetic acid in the ratio `a:n` and another hydrogen electode Y was placed in a buffer solution of sodium acetate and acetic acid in the ratio `b:a`. If reduction potential values for two cells are found to be `E_(1)` and `E_(2)` respectively w.r.t standard hydrogen electrode, the `pK_(a)` value of the acid can be given as:A. `(E_(1) + E_(2))/(0.118)`B. `(E_(2) - E_(1))/(0.118)`C. `(-E_(1) + E_(2))/(0.118)`D. `(E_(1) - E_(2))/(0.118)`

Answer» Correct Answer - A
2439.

Given standard electode potenitals ` Fe^(2+) + 2e^(-) rarr Fe, E^@ =- 0. 44 V ` ………………(1) ` Fe^(3+) + 2e^(-) rarr Fe, E^@ =- 0. 036 V` ………….(2) The standard electrode pptential `E^@ ` for `Fe^(2+) + e rarr Fe^(2+)` is.A. ` -0. 476 V`B. ` -0. 404 V`C. `0. 404 V`D. ` +0. 772 V`

Answer» Correct Answer - D
`Fe^(2+) + 2e rarr Fe, DeltaG_1^@ =- nE^2 F=- 2 F (-0.44)`
`= 0.88 F`
`Fe^(2+) + 2e rarr Fe, DeltaG_2^@ =- nE^2 F=- 2 F (-0.036)`
` =0.108 F`
On subtracting (1) from (2)
`Fe^(3+) +d^- rarr Fe^(2+)` or `Delta G =- 0. 772 F`
or ` Delta G =- nE^@ F=- 0.772F`
Or ` E^@ = (0.772 )/1 -.0772 V`.
2440.

What is the effect of temperature on the rate constant ?

Answer» Most of the chemical reactions are accelerated by increased of temperature.
`to` For a chemical with rise of temperature by `10^(@)C` the rate constant is nearly doubled
`k=A.e^(-Ea//RT)`
2441.

In electrolysis of `NaCl` when `Pt` electrode is taken `H_(2)` is liberated at cathode while `Hg` cathode it forms sodium amalgam becauseA. Hg ismore inert than PtB. More voltage is required to reduce `H^(+)` at Hg than at Pt.C. Na is dissolved in Hg while it does not dissolve in PtD. Conc. Of `H^(+)` ions is larger when Pt electrode is taken.

Answer» Correct Answer - B
More voltage is required to reduc e `H^(+)` at Hg than at Pt.
2442.

In electrolysis of `NaCl` when `Pt` electrode is taken `H_(2)` is liberated at cathode while `Hg` cathode it forms sodium amalgam becauseA. Hg is more inert than PtB. more voltage is required to reduce `H^(+)` at Hg than at PtC. Na is dissovled in Hg while it does not dissolved in PtD. concentration of `H^(+)` ion is larger when Pt electrode is taken

Answer» Correct Answer - B
(b) Sodium Chloride in water dissociates as
`NaCl iff Na^(+) +Cl^(-)`
`H_(2)O iff H^(+) +OH^(-)`
When electric current is passed through this solution using platinum eletrodes , `Na^(+) and H^(+)` move towards cathode whereas `Cl^(-) and OH^(-)` ions move towards anode.
At cathode
`H^(+)+e^(-) to H`
`H+H to H_(2)`
At anode
`Cl^(-) to Cl+e^(-)`
`Cl+Cl to Cl_(2)`
If mercury is used as cathode, `H^(+)` ions are not discharged at mercury cathode because mercury has high hydrogen over voltage. `Na^(+)` ions are discharged at cathode in preference of `H^(+)` ions yielding sodium, which dissolves in mercury to form sodium amalgum.
2443.

In electrolysis of `NaCl` when `Pt` electrode is taken `H_(2)` is liberated at cathode while `Hg` cathode it forms sodium amalgam becauseA. `Hg` is more insert than `Pt`B. More valtage is required to reduce `H^(+)` at `Hg` than at `Pt`C. `Na` is dissolved in `Hg` while it does not dissolve in `Pt-`D. Concentration of `H^(+)` ions is larger when `Pt` electrode is taken

Answer» Correct Answer - B
`NaCl(aq.) rarr Na^(+)(aq.)+Ci^(-)`
At cathode
`Na^(+)(aq.)+e^(-) rarr Na(s)`
or `2H_(2)O(l) rarr O_(2)(g)+4H^(+)(aq.)+4e^(-)`
When `Pt` electrode is used, `H_(2)O` is reduced as its reduction potential is higher than that of `Na^(+)` ions. However, due to over-voltage for the liberation of `H_(2)(g)` at `Hg` electrode, the `H^(+)` ions arc not discharged at `Hg` cathode. Thus, `Na^(+)` ions are discharged at cathode (in perference of `H^(+)` ions) yielding `Na` metal, which dissolves in `Hg` to form sodium amalgam.
2444.

Calculate emf of the following cell Cd/Cd2+ (.10 M)//H+ (.20 M)/H2 (0.5 atm)/Pt [Given E° for Cd2+ /Cd = -0.403 v]

Answer»

Ecell = E°cell – 0.0591/n Log [Cd2+]/ [H+]2 

 E°cell = 0 – (–.403 V) =0.403 V 

= 0.0403 – 0.0591/2 Log (0.10) X 0.5/(0.2)2 = 0.400 V 

2445.

The `EMF` of a galvanic cell `Pt|H_(2)(1 atm)|HCl(1M)|Cl_(2)(g)|Pt` is `1.29V`. Calculate the partial pressure of` Cl_(2)(g)`. `E^(c-)._(Cl_(2)|Cl^(c-))=1.36V`.

Answer» Cell reaction `:`
`(1)/(2)H_(2)(g)rarr 2H^(o+)+e^(-)" "E^(c-)._(o x i d)=0V`
`2Cl_(2)(g)+e^(-) rarr Cl^(c-)(aq)" "E^(c-)._(red)=1.36V`
`ulbar((1)/(2)H_(2)(g)+(1)/(2)Cl_(2)(g)rarrH^(o+)(aq)+Cl^(c-)(aq)" "E^(c-)._(cell)=1.36V)`
`E_(cell)=E^(c-)._(cell)-(0.059)/(1) log.([H^(o+)][Cl^(c-)])/([P_(H_(2))]^(1//2)[P_(Cl_(2))]^(1//2))`
`1.29=1.36-(0.059)/(1)log ((1xx1)/(1xx[p_(Cl_(2))]^(1//2)))`
Solve, `p_(Cl_(2))=4.24xx10^(-3)atm`
2446.

In a lead storag battery, Pb (anode) and `PbO_(2)` (cathode) are used. Concentrated `H_(2)SO_(4)` is used as electrolyte. The battery holds 3.5 litre acid with it . In the discharge process, the density of acid fell from 1.294 to 1.139 g/mL. The sulphuric acid of density `1.294" g mL"^(-1)` is 39 % by mass and that of density 1.139 g/mL is 20% by mass. The amount of charge which the battery must have been used is :A. 9.88 FB. 8.98 FC. 8.89 FD. 7.88 F

Answer» Correct Answer - A
2447.

The passage of current through the solution of a dcertain electrolyte results in the liberation of `H_(2)` at the cathode and chlorine at the anode. The solution in the container could be:A. `NaCl(aq.)`B. `CuCl_(2)(aq.)`C. `Kcl(aq.)`D. `MgCl_(2)(aq.)`

Answer» Correct Answer - A::C::D
2448.

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Answer»

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2449.

`EMF` of the cell `Zn ZnSO_(4)(a =0.2)||ZnSO_(4)(a_(2))|Zn` is `-0.0088V` at `25^(@)C`. Calculate the value of `a_(2)`.

Answer» Correct Answer - `a_(2) = 0.1006M`
`E_(cell) = (0.0591)/(2)log.([0.2])/([a_(2)])`
`(-0.0088 xx 2)/(0.0591) =- log. ([0.2])/([a_(2)])`
`10^(+0.3) = (0.2)/(a_(2))`
`a_(2) = 0.1006`
2450.

Calculate the `EMF` of a Daniel cell when the concentartion of `ZnSO_(4)` and `CuSO_(4)` are `0.001M` and `0.1M` respectively. The standard potential of the cell is `1.1V`.

Answer» Correct Answer - `E = 1.158V`
`E_(cell) = (E_(cell)^(@) - (0.0591)/(2) log .([Zn^(2+)])/([Cu^(2+)]))`
`= 1.1 -(0.0591)/(2)log.([10^(-3)])/([10^(-1)])`
`= 1.1 +0.0591` ltbr. `=1.1591V`