Self Studies

Chemical Kinetics Test - 66

Result Self Studies

Chemical Kinetics Test - 66
  • Score

    -

    out of -
  • Rank

    -

    out of -
TIME Taken - -
Self Studies

SHARING IS CARING

If our Website helped you a little, then kindly spread our voice using Social Networks. Spread our word to your readers, friends, teachers, students & all those close ones who deserve to know what you know now.

Self Studies Self Studies
Weekly Quiz Competition
  • Question 1
    1 / -0
    A reaction takes place in thee steps.The rate constants are $$K_1,K_2$$ and $$k_3$$. The over all rate constant $$k=\cfrac{K_1K_3}{K_2}$$. If (energy of activation) $$E_1, E_2$$ and $$E_3$$ are $$100, 20$$ and $$40 kJ$$.The overall energy of activation is:
  • Question 2
    1 / -0
    In a reaction carried out at 400 k, $$0.0001\%$$ of the total number of collisions are effective. The energy of activation of the reaction is:
    Solution
    We know that, Arrhenius equation for calculation of energy of activation of reaction with rate constant $$K$$ and temeperature $$T$$ is 
    $$K=A$$ $$e^{-Ea/RT}$$
    where, $$Ea$$= Arrhenius activation energy
    $$A$$= pre exponential factor (frequency factor)

    Now, $$e^{-Ea/K_BT}$$= Fraction of collision having more than activation energy
    where, $$K_B=$$ Boltzmann constant
    Given, $$T=400$$ $$K$$       and effective collision= $$0.0001$$%

    $$\Rightarrow$$ Effective Collision= $$e^{-Ea/K_BT}$$
    $$\Rightarrow$$ $$0.0001$$%= $$e^{-Ea/1.3\times 10^{-23}\times 400}$$
    $$\Rightarrow$$ $$10^{-6}$$= $$e^{-Ea/1.3\times 10^{-23}\times 400}$$

    $$\Rightarrow$$ $$2.303\times \log 10^{-6}$$= $$\cfrac {-Ea}{1.3\times 10^{-23}\times 400}$$
    $$\Rightarrow$$ $$2.303\times (-6)$$= $$\cfrac {-Ea}{1.3\times 10^{-23}\times 400}$$

    $$\Rightarrow$$ $$Ea$$= $$1.3\times 10^{-23}\times 400\times6\times 2.303=7.19\times 10^{-20}$$ $$J/mol$$
  • Question 3
    1 / -0
    What is the activation energy for a reaction if its rate doubles when the temperature is raised from $$20^{\circ}C$$ to $$35^{\circ}C$$?
    Solution

    $$K_2=2K_1, T_2=35+273=308$$ $$K, T_1=20+273=293$$ $$K$$

    $$\ln \cfrac {K_2}{K_1}=\cfrac {E_a}{R}\left [\cfrac {1}{T_1}-\cfrac {1}{T_2}\right]$$

    $$\therefore \ln 2=\cfrac {E_a}{8.314}\left[\cfrac {1}{293}-\cfrac {1}{308}\right] $$

    $$\therefore \cfrac {8.314\times \ln 2}{(3.41-3.24)\times 10^{-3}}=E_a$$

    $$\therefore E_a\approx 34.7$$ $$kJ/mol$$

  • Question 4
    1 / -0
    At a certain temperature, the first order rate constant $$k_{1}$$ is found to be smaller than the second order rate constant $$k_{2}$$. If $$E_{a}(1)$$ of the first order reaction is greater than $$E_{a}(2)$$ of the second order reaction, then as temperature is raised:
    Solution

  • Question 5
    1 / -0
    For the following reaction at a particular temperature, according to the equations,
    $$ 2N_2O_5 \rightarrow 4NO_2 + O_2 $$ 
    $$2NO_2+1/2O_2 \rightarrow N_2O_5$$
    the activation energies are $$E_1$$ and $$E_2$$ respectively, then:
    Solution

  • Question 6
    1 / -0
    A substance $$A$$ undergoes decomposition in solution following the first order kinetics. Flask $$I$$ contains 1 litre of 1 M solution of $$A$$ and flask $$II$$ contains $$100$$ $$ml$$ of 0.6 M solution. After 8 hours, if the concentration of $$A$$ in flask $$I$$ became 0.25 M, what will be the time required in hours for the concentration of $$A$$ in flask $$II$$ to become 0.3 M?
    Solution
    Initial concentration of $$A$$= $$1M$$
    Concentration after $$2$$ hours= $$0.25M$$
    Since, the reaction follows first order kinetics; so, time taken to have concentration  $$0.5M=4$$ hours

    This is half life $$t_{1/2}$$ of the reaction.
    $$\Rightarrow$$ $$t_{1/2}=4$$ hours

    Now in Flask II
    Initial concentration of $$A=0.6M$$
    Final concentration of $$A=0.3M$$

    Since, the concentration is reduced to half of its initial value so time required for it to happen will be $$t_{1/2}$$ i.e. $$4$$ hours.
  • Question 7
    1 / -0
    It takes $$1\ h$$ for a first order reaction to go to $$50$$% completion. The total time required for the same reaction to reach $$87.5$$% completion will be:
    Solution
    For first order reaction we have:-
    $$K=\cfrac {1}{t} ln \left(\cfrac {a}{a-x}\right)$$                 $$- (i)$$

    where, $$K$$= rate constant
                 $$t$$=time
                 $$a$$= initial concentration of the reactant
                 $$x$$= amount of reactant reacted in time $$t$$

    Case I:- $$t=1$$ hour & $$x=0.5a$$
    $$(a-x)=0.5a$$

    Putting the values in $$(i)$$:-
    $$K=\cfrac {1}{1} ln \left(\cfrac {1}{0.5}\right)= ln 2$$       $$- (ii)$$

    Case II:- $$t=?$$ & $$x=0.875a$$
    $$(a-x)=0.125a$$

    Putting the value in $$(ii)$$:-
    $$K=\cfrac {1}{t} ln \left(\cfrac {1}{0.125}\right)=\cfrac {1}{t} ln (8)$$      $$- (iii)$$

    From, $$(ii)$$ and $$(iii)$$ $$\Rightarrow ln2=\cfrac {1}{t} ln 8$$
    $$\Rightarrow t=\cfrac {ln8}{ln2}=3$$ hours       $$[\because ln(2^3)=3ln2]$$
  • Question 8
    1 / -0
    Calculate the rate constant for decomposition of ammonium nitrate from the following data;
    $$NH_4NO_2\rightarrow N_2+2H_2O$$
    Time (minutes)1025$$\infty$$
    Vol.of $$N_2$$ ml6.2513.6535.05
    Given that the reaction follows first order kinectics.
    Solution
    The decomposition of ammonium nitrate is given by 
    $$NH_4NO_2\longrightarrow N_2+2H_2O$$

    The kinetics of this reaction is studied by measuring volume of $$N_2$$ formed at different intervals.

    Let, $$V_\infty$$ denotes volume of $$H_2$$ formed at $$\infty$$ time.
                                            (time at which reaction is complete)

    $$\Rightarrow$$ $$V_\infty \propto$$ amount of $$NH_4NO_2$$ present initially  $$(a)$$
    $$\Rightarrow$$ $$V_\infty \propto a$$        $$- (i)$$
    Let, $$Vt$$ is the volume of $$N_2$$ at any time $$t$$.

    $$\Rightarrow$$ $$Vt\propto$$ amount of $$NH_4NO_2$$ reacted $$(x)$$
    $$\Rightarrow$$ $$Vt\propto x$$       $$- (ii)$$

    Now, $$(a-x)\propto (V_\infty-Vt)$$     $$- (iii)$$

    Now, since this reaction follows first order kinetics, so, 
    $$K=\cfrac {1}{t} ln \left(\cfrac{a}{a-x}\right)$$          $$- (iv)$$

    where, $$K$$= rate constant, $$t$$= time, $$a$$= initial concentration of reactant, $$x$$= amount of reactant reacted in time $$t$$

    Putting (i) & (iii) in (iv):-
    $$K=\cfrac {1}{t} ln \left(\cfrac {V_\infty}{V_\infty-Vt}\right)$$       $$- (v)$$

    According to question, $$V_\infty=a=35.05$$

    Now, at $$t=10$$ min, $$V_t=6.25$$ ml

    Putting the values in $$(v)$$ :-
    $$K=\cfrac {1}{10} ln \left(\cfrac {35.05}{35.05-6.25}\right)$$
    $$=\cfrac {1}{10} ln \left(\cfrac {35.05}{20.00}\right)$$
    $$=\cfrac {1}{10} ln (1.22)=\cfrac {1}{10}\times 0.1900$$
    $$=0.01900$$ $$min^{-1}$$
  • Question 9
    1 / -0
    The spontaneous decomposition of radio nuclei is a first order rate process.U-238 disintegrates with the emission of $$\alpha$$-particles and has a half-life of $$4.5 \times 10^9$$ years. If at time t=0, 1 mole of U-238 is present, what will be the number of nuclei left after 1 billion years?
    Solution
    We know that,
    Radioactive disintegration follows first order kinetics.
    Now, half life period of a reaction is the time taken by reaction to be half completed.
    So, amount of reactant left after one half life period= $$\cfrac {[A]_0}{2}$$ ; $$A_0$$ is the amount present at $$t=0$$

    Amount present after $$2$$ half lines= $$\cfrac {[A]_0}{2^2}$$
    In general, amount of reactant left after $$n$$ half lives=$$\cfrac {[A]_0}{2^n}$$

    Now, Half life of $$U-238=4.5\times 10^{9}$$ yrs
    Given time, $$t=1$$ billion years
                           $$=10^{9}$$ years

    So, no. of half lives=$$\cfrac {10^9}{4.5\times 10^9}=\cfrac {1}{4.5}$$
    Amount of reactant left= $$\cfrac {[A]_0}{2^{4.5}}$$
    =$$\cfrac {[A]_0}{22.68}$$

    Now, at $$t=0$$, amount of $$U-238$$ present= $$1$$ mole=$$6.022\times10^{23}$$ molecules (nuclei)

    $$\therefore$$ No. of nuclei left after $$1$$ billion years= $$\cfrac {6.022\times 10^{23}}{22.68}$$
    $$=0.27\times 10^{23}$$
  • Question 10
    1 / -0
    For the equilibrium, $$A(g) \rightleftharpoons B(g), \triangle H$$ is $$-40\ kJ/mol$$. If the ratio of the activation energies of the forward $$(E_{f})$$ and reverse $$(E_{b})$$ reactions is $$2/3$$ then:
    Solution
    The given reaction is,
    $$A(g)\rightleftharpoons B(g)$$
    $$\triangle H= -40 KJ/mol$$
    & $$\cfrac {E_f}{E_b}=\cfrac {2}{3} \Rightarrow E_f=\cfrac {2}{3} E_b$$
    From graph we have,
    $$\triangle H=E_b-E_f$$
    $$\Rightarrow -40=E_b-\cfrac {2}{3}E_b$$
    $$\Rightarrow -40= \cfrac {1}{3}E_b \Rightarrow E_b=-120 KJ/mol$$
    & $$E_f=E_b-\triangle H$$
    $$=-120- (-40)$$
    $$-80$$ $$KJ/mol$$.
Self Studies
User
Question Analysis
  • Correct -

  • Wrong -

  • Skipped -

My Perfomance
  • Score

    -

    out of -
  • Rank

    -

    out of -
Re-Attempt Weekly Quiz Competition
Selfstudy
Selfstudy
Self Studies Get latest Exam Updates
& Study Material Alerts!
No, Thanks
Self Studies
Click on Allow to receive notifications
Allow Notification
Self Studies
Self Studies Self Studies
To enable notifications follow this 2 steps:
  • First Click on Secure Icon Self Studies
  • Second click on the toggle icon
Allow Notification
Get latest Exam Updates & FREE Study Material Alerts!
Self Studies ×
Open Now