The question is incomplete, here is the complete question:
The rate constant of a certain reaction is known to obey the Arrhenius equation, and to have an activation energy Ea = 71.0 kJ/mol . If the rate constant of this reaction is 6.7 M^(-1)*s^(-1) at 244.0 degrees Celsius, what will the rate constant be at 324.0 degrees Celsius?
<u>Answer:</u> The rate constant at 324°C is 
<u>Explanation:</u>
To calculate rate constant at two different temperatures of the reaction, we use Arrhenius equation, which is:
![\ln(\frac{K_{324^oC}}{K_{244^oC}})=\frac{E_a}{R}[\frac{1}{T_1}-\frac{1}{T_2}]](https://tex.z-dn.net/?f=%5Cln%28%5Cfrac%7BK_%7B324%5EoC%7D%7D%7BK_%7B244%5EoC%7D%7D%29%3D%5Cfrac%7BE_a%7D%7BR%7D%5B%5Cfrac%7B1%7D%7BT_1%7D-%5Cfrac%7B1%7D%7BT_2%7D%5D)
where,
= equilibrium constant at 244°C = 
= equilibrium constant at 324°C = ?
= Activation energy = 71.0 kJ/mol = 71000 J/mol (Conversion factor: 1 kJ = 1000 J)
R = Gas constant = 8.314 J/mol K
= initial temperature = ![244^oC=[273+244]K=517K](https://tex.z-dn.net/?f=244%5EoC%3D%5B273%2B244%5DK%3D517K)
= final temperature = ![324^oC=[273+324]K=597K](https://tex.z-dn.net/?f=324%5EoC%3D%5B273%2B324%5DK%3D597K)
Putting values in above equation, we get:
![\ln(\frac{K_{324^oC}}{6.7})=\frac{71000J}{8.314J/mol.K}[\frac{1}{517}-\frac{1}{597}]\\\\K_{324^oC}=61.29M^{-1}s^{-1}](https://tex.z-dn.net/?f=%5Cln%28%5Cfrac%7BK_%7B324%5EoC%7D%7D%7B6.7%7D%29%3D%5Cfrac%7B71000J%7D%7B8.314J%2Fmol.K%7D%5B%5Cfrac%7B1%7D%7B517%7D-%5Cfrac%7B1%7D%7B597%7D%5D%5C%5C%5C%5CK_%7B324%5EoC%7D%3D61.29M%5E%7B-1%7Ds%5E%7B-1%7D)
Hence, the rate constant at 324°C is
Answer:
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<h3><u>c) 13.29 mL</u></h3>
The answer is B
Homozygous mean the same and you know that the two alleles will be the same (either BB or bb) and receive is usually the lower case set of alleles
Answer:
7,94 minutes
Explanation:
If the descomposition of HBr(gr) into elemental species have a rate constant, then this reaction belongs to a zero-order reaction kinetics, where the r<em>eaction rate does not depend on the concentration of the reactants. </em>
For the zero-order reactions, concentration-time equation can be written as follows:
[A] = - Kt + [Ao]
where:
- [A]: concentration of the reactant A at the <em>t </em>time,
- [A]o: initial concentration of the reactant A,
- K: rate constant,
- t: elapsed time of the reaction
<u>To solve the problem, we just replace our data in the concentration-time equation, and we clear the value of t.</u>
Data:
K = 4.2 ×10−3atm/s,
[A]o=[HBr]o= 2 atm,
[A]=[HBr]=0 atm (all HBr(g) is gone)
<em>We clear the incognita :</em>
[A] = - Kt + [Ao]............. Kt = [Ao] - [A]
t = ([Ao] - [A])/K
<em>We replace the numerical values:</em>
t = (2 atm - 0 atm)/4.2 ×10−3atm/s = 476,19 s = 7,94 minutes
So, we need 7,94 minutes to achieve complete conversion into elements ([HBr]=0).
It’s lower, hope this helps with your issue and helps solve your problem, no problem
