Types of Elementary Reactions
Trending Questions
How to balance chemical equations?
(Use: ln 2=0.693)
- The rate constant, k, of the reaction is 13.86×10−4 s−1
- Half-life of X is 50 s
- At 50 s, −d[X]dt=13.86×10−4 molL s−1
- At 100 s, −d[Y]dt=3.46×10−3 molL s−1
In a reaction if the concentration of reactant A is tripled, the rate of reaction becomes twenty seven times. What is the order of the reaction?
The unit of rate constant of first-order reaction is _________
- 300 seconds
- 500 seconds
- 5000 seconds
- 3000 seconds
For which of the following order unit of rate of reaction and rate constant are the same?
First-order reaction
Second-order reaction
Third-order recation
Zero-order reaction
If the rate of disappearance of I– is 9/2×10–3 mol/L−1 s−1, what is the rate of formation of SO2−4 during the same time?
- 10−3 mol/L−1 s−1
- 2×10−3 mol L−1 s−1
- 3×10−3 mol L−1 s−1
- 4×10−3 mol L−1 s−1
For the elementary reaction M → N, the rate of disappearance of M increases by a factor of 8 upon doubling the concentration of M. The order of the reaction with respect to M is
- 4
- 3
- 1
- 2
- 1
- 0
- 2
- 3
(b) The rate constant of a first order reaction increases from 4×10−2 to 8×10−2 when the temperature changes from 27∘C to 37∘C.
Calculate the energy of activation (Ea). (log 2 =0.301, log 3 =0.4771, log 4 =0.6021)
For a reaction A+B⟶ Products, the rate law is ---Rate = k[A][B]3/2 Can the reaction be an elementary reaction? Explain.
Which of the following statements are applicable to a balanced chemical equation of an elementary reaction?
(a) Order is same as molecularity
(b) Order is less than the molecularity
(c) order is greater than the molecularity
(d) Molecularity can never be zero
The rate of first-order reaction is at and at after initiation of the reaction. What is the half-life period of the reaction?
- Molecularity for a particular reaction can be fractional
- Order for a particular reaction can be fractional
- Molecularity is defined for elementary reactions only.
- Order of a reaction is a theoretical value.
[Where r = rate of reaction;
[A]1=Concentration at time t1;[A]2=Concentration at time t2
- lnr2−lnr1ln[A]2−ln[A]1
- ln[A0]2−ln[A0]1ln[t1/2]−ln[t1/2]1
- ln(−d[A]k.dt)/ln[A]
- ln(r/k)ln[A]
- Rate of forward reaction is always very large.
- Rate of backward reaction is very slow in the end.
- Rate of forward reaction is very large at the beginning.
- Rate of backward reaction is very slow in the beginning.
- 2×104
- 3.45×10−5
- 1.386×10−4
- 2×10−4
- The value of d[C]dt=2×10−2[A], where [specie] represents concentration of specie at time t
- The value of d[C]dt=8×10−2[A], where [specie] represents concentration of specie at time t
- Rate at which B is being formed is 1.5 times the rate at which A is decomposing
- Pressure of the gases would never be double of the original in a finite interval of time keeping volume and temperature constant
- 5.21×10−3 min−1
- 5.12×10−3 min−1
- 5.89×10−3 min−1
- None of these
- 48min
- 50min
- 46min
- 45min
- 2.303 Mmin−1
- none ofthese
- 0.2303 Mmin−1
- 0.1 Mmin−1
- 0.01 mol L−1min−1
- 0.04 mol L−1min−1
- 0.05 mol L−1min−1
- 0.03 mol L−1min−1
- 0.02 mol L−1min−1
Suggest some ways to balance an equation?
- 20.4 minutes
- 21.6 minutes
- 30.2 minutes
- 26.7 minutes
- 924 sec
- 462 sec
- 1848 sec
- none of these
- 2.50×10−4molL−1s−1
- 1.25×10−4molL−1s−1
- 3.75×10−4molL−1s−1
- 5.00×10−4molL−1s−1
- Avogadro
- Guldberg-Waage
- Michelles-Menten
- None of these
C2H5Cl(g)hv→C2H4(g)+HCl(g)
Time (sec) Total pressure (atm)
0 0.30
300 0.50
Calculate the rate constant.(Given: log 2 = 0.301, log3 = 0.4771, log 4 = 0.6021)
[A] (mol/L) | rate (mol/L.s) |
0.250 | 3.40×102 |
0.500 | 1.36×103 |
1.00 | 5.44×103 |
- Rate = 5.44×103[A]2
- Rate = 1.36×103[A]2
- Rate = 5.44×103[A]
- Rate = 1.36×103[A]