Chemistry, asked by rakeshkhadkya90, 10 months ago

1. Choose the most correct option.
A. A sample of pure water, whatever the source always contains .......... by mass of oxygen and 11.1 % by mass of hydrogen .
a. 88.8 b.18 c.80 d.16
B. Which of the following compounds can NOT demonstrate the law of multiple proportions?

Answers

Answered by vandanatripathi717
1

Answer:

64 kJ mol

1

Explanation:

Your tool of choice here will be the Arrhenius equation, which looks like this

¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯

a

a

k

=

A

exp

(

E

a

R

T

)

a

a

−−−−−−−−−−−−−−−−−−−−−−−−

, where

k

- the rate constant for a given reaction

A

- the pre-exponential factor, specific to a given reaction

E

a

- the activation energy of the reaction

R

- the universal gas constant, useful here as

8.314

J mol

1

K

1

T

- the absolute temperature at which the reaction takes place

As you can see, the Arrhenius equation establishes a relationship between the rate constant and the absolute temperature at which the reaction takes place.

In other words, this equation allows you to determine how a change in temperature affects the rate of the reaction.

Now, convert the two temperatures from degrees Celsius to Kelvin by using the conversion factor

¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯

a

a

T

[

K

]

=

t

[

C

]

+

273.15

a

a

−−−−−−−−−−−−−−−−−−−−−−−−

You will thus have

T

1

=

100

C

+

273.15

=

373.15 K

T

2

=

150

C

+

273.15

=

423.15 K

So, you know that at

T

1

, the rate constant for your reaction takes the form

k

1

=

A

exp

(

E

a

R

T

1

)

Likewise, at

T

2

the rate constant takes the form

k

2

=

A

exp

(

E

a

R

T

2

)

Divide these two equations to get rid of the pre-exponential factor,

A

k

1

k

2

=

A

exp

(

E

a

R

T

1

)

A

exp

(

E

a

R

T

2

)

This will be equivalent to - using the properties of exponents

k

1

k

2

=

exp

[

E

a

R

(

1

T

2

1

T

1

)

]

Take the natural log of both sides of the equation to get

ln

(

k

1

k

2

)

=

E

a

R

(

1

T

2

1

T

1

)

Rearrange to solve for

E

a

, the activation energy of the reaction

¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯

a

a

E

a

=

R

ln

(

k

1

k

2

)

1

T

2

1

T

1

a

a

−−−−−−−−−−−−−−−−−−−−

Finally, plug in your values to get

E

a

=

8.314 J mol

1

K

1

ln

(

1.3

10

4

M

1

s

1

1.5

10

3

M

1

s

1

)

(

1

423.15

1

373.15

)

K

1

E

a

=

64,212.3 J mol

1

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