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Class 12 Chemical Kinetics Guide

Chemical kinetics is the branch of chemistry that deals with the study of reaction rates and their mechanisms. The rate of a reaction is defined as the change in molar concentration of a reactant or product per unit time. Average rate of reaction can be calculated using the change in concentration of a reactant or product over a time interval. For example, if the concentration of reactant A decreases from 0.5 mol/L to 0.4 mol/L in 10 minutes, the average rate of reaction is 0.001 mol/L/min.
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100% found this document useful (1 vote)
3K views12 pages

Class 12 Chemical Kinetics Guide

Chemical kinetics is the branch of chemistry that deals with the study of reaction rates and their mechanisms. The rate of a reaction is defined as the change in molar concentration of a reactant or product per unit time. Average rate of reaction can be calculated using the change in concentration of a reactant or product over a time interval. For example, if the concentration of reactant A decreases from 0.5 mol/L to 0.4 mol/L in 10 minutes, the average rate of reaction is 0.001 mol/L/min.
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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CLASS -12 .

Chemical
kinetics

Designed by 2¥ Bharat Panchal


-

Bharat Panchal Sir


-
bharat pancha 192 . . .
4. Chemical
kinetics . . .

Branch of chemistry that deals with the study


of reaction rates and their mechanisms .


Rate of Reaction change in molar conc .

of reactant or
product per unit time
R →p

Rale =
-
A ER] or 1- AID
It At

Unit
molarcohc.GRorp-mol.tl sect
Time taken or atm sect
for gaseous Rin

1¥ Average rate of Rxn * Instantaneous rate of Rxn

Change in molar conc .

of change in molar conc .

R or P of R or P at a
particular
during a large instant of time
interval of time
R → p
tax
ACaIf tins
doffs tddf
-

then
-
-
.
- =
. . =
.

aAtb B → cc
sins"
ha dde¥
-
=

""
ta AEE Ig a¥z3=+za¥¥
-
-
=

tf dat?
=
'

=
-5%17 .

:÷dE÷.si:8?..mT
-

Thi
2X t 34 → 52

rate of reaction t deff Idea'T -1¥ deaf


-
-
= = =

rate of disappearance of X = -
dad
dt
rate of disappearance of Y = -
dad
at
rate of appearance of 2 = + DI
dt
ONCE MIN a reaction , 2A → Product the of A decreases from
,
conc .

0.5 Mol L I to 0.4 moi ti in Lo min Calculate the rate


during
-

this interval .

AE AEAI
Average rate = -

I At
) 005 mol.tl mint
I ¥-15
o
I
-

- -

= = =

=
5×10-3 mo LL I mini -
'

"
"
Q A -13 B → 2C, the rate of formation of C is 2.5×10-4 mol L -
is -
I

calculate the
Ci ) rate of reaction ( ii) rate of disable .

of B

Ans 2.5×10-4 moths


Given rate of formation of C
tdd# I
-
.
=
, =

of
fddeAf=-tzda¥=tIdaI
race reaction -

- -

rate
ci ,
of reaction
+
Iz DEI 21×2.5×10-4
=

dt
1.25×10-4
=
moths -
I

Cii ) Rate of disappearance of B


doffed Zdd¥
-
= =

3.75×10-4 Molle sect


=
3-2×2.5×104 =

92018 2 Ngos → 4 NO
, -102 ,
the rate of formation of NO ,

is 2.8×153 Ms - i .
Calculate the rate of dis .
Of Ncos .

A 2.8×103 Ms
Given , sale of formation NO
DINO
]
of
- '

, , =

of reaction
I dialed
rate

ttdzfd.de#a0s-3--EdTdNf
tf death
-

, =
=

? I +2.8×10-3=1.4×10-3 Ms -

I
Fatties
mmmm

C- influencing rate of a reaction


www.ww-wwww-w
www-
25

concentration -

Greater the conc . of reactants faster is


,
the rate of reaction .

*
Physical state of Reactant -

Reactions
reactants involving gaseous
are faster than reactions
containing solid
and
liquid reactants .

Temperature -

The race of reaction increases with increase


of temperature , for most of the reactions rate of reaction ,

becomes almost doubles with


every ios rise in tents .

¥ Presence of catalyst
A catalyst generally increases the
speed of reaction .

* Surface Area of Reactant -

Greater the surface area


of reactant
,
faster is the reaction .

# Presence of light -

Those reaction which takes


place
in the presence of sunlight, called photochemical Rxn
* Activation Energy -

lower the activation energy faster


is the reaction .

Rate law
murmur

rate of reaction
to the
is
directly prop.

product of molar conc .

of reactant and each


raise to the power their conc .
term on which rate of
reaction actually depends .

AA + BB → Product
s s
actual used a
B
"
B
rate of reaction X CA] CB]
rate of reaction = K CAT CB ] ?
K -7 rate constant or specific reaction rate

rate constant is defined as the rate of reaction when


molecular all the
conc of . reactants is
unity .

Q Define order of reaction .

Ads .

AA + BB → Product It is the sum of the


3 } powers on conc . terms
& B
of all the reactants acc .

rate ACA)
'
CBTB to rate law expression .

9 → wir 't A Bt
w.r.tBP.TT
order =
At B ,

order of a reaction can be 0,112,3 $ even fractional .

"' I
-

Give order of reaction r = KEAT (B) order =


312
f- KC A) ZEB] Order =3

MIIKE Unit of rate constant for different order

K= (Mol L
- '
7th Sec I
-

'
hsec
-

Zero order K ( Mol L D i


Moll I
see I
-
- - -

- -

' '
first (Moll D Sec i
-

order K Sec I
-
- - -
-

(Moll D -2 Sec
'
Second Order K Mol Il
"
-
= -
-
I see

Difference between Order and


- - - - Molecularity
-

E*
Q .
For a reaction At B →D
,
the sate is given by
zale =
KEAT E B) 2

cis How is the rate of reaction affected it conc .

of B is doubled ( C. B.S E .
-
2015 )

Ciii what is the overall order of reaction it A is


present in large excess .

Anse ATB → p
2
Rate of reaction a- KCAIEB]
If conc .

of B is doubled 81 = KEAT CLB) 2


?
-
=
4 KCAIEB]
81=4×21
rate of reaction ,
becomes a times

dig rate of reaction ,


F- KEAT CBH
& A b present in large excess , the race law becomes
'd
8 = K '
EBI The overall order b two .

Q .
For a Rxh
2MHz # Na +3112
rate =
K

cis write the order $ molecularity of Rxn
cii , write the unit
of K

An Cil Order
given reaction b
of the zero but its
molecularity is two '
Lt ) Tec
-

Cii , since the order is two , Kemal -


I

= MOLLY sect

① Give order 90420120 order = o


I
K L mo I
I
-

see
-
=

=L
K = L mot
'
Sec
-
e

ATT Uf got Power E stent


T -
bat AT
vets
IT L

1 dnt I order 31T NIM

NinjaTipuM writing 23¥ speed ATE ,

Q write two factors which a Hed


-
-

rate of reaction
Ans Cil Temp dig catalyst Ciii ) surface Area .
.
IfnkgoatedRakEqnT
we were

first Order
- -
Those reactions which depends upon
one conc . term of reactant

R → P
Rate a R
'
-
d KERI
=
hat sit Down
-
der) Kdt
=

Try
both Sides
Integrating
SDI} kfdt integration
-
=

#
1-
In CR)
-

I
①-
= Kt 1- -
constant

j feel drei # 4Th Lahti

Tofyget
the I value of

iE¥Et put value of I

mea.io
-
In CR ] -
- Kt -
en Ro

en Ro -
lnR= Kt E. log x -
logy
en
Roz Kt
engage ]
=
=

£303 log If = Kt C- : ln =L 303-

log]

&3sETnEuTp- Caba
for Numerical
E-
23,91 log a- a K -

A -7 initial conc .
A K → conc
- .
left behind
.
a

{www
Zero Order Those
-

dent
reactions
on the
which are indepen
reactant
.

conc of
.
.

R → P

Rate of Reaction a CRJ


dead-

K =
AM
Both?
dt C
DCR) K dt ( Integrating ,

desert
-
-
-

www
-

Sd CR)
Kfdt =

Itry ME integrationconstant
# ②
To the value of I
get

try
|E,
put value
of I in
eq①
-

R = Kt -
Ro

- - - -

order )
Ro -
R = Kt
Ridged
1-Hal flifepeoiodctiIIt.is
Graph of Zero

in
I
the time which
- half of the reactant
'
reduced
T -1 Et
first order Zero order
1- = R = Ro 12 E- tyz R Rel z
tyz
-
-

,
,

Rod
t
23,03T log Rs t -
.
-
-

K
R

tye Ro Rs
tyz
Rez.x2
-

2.3%3
=

log
-
-

Z
-

±@L K Fierst
D@IuForgetuT half
on
life of first order is
the initial conc .
independent
of reactant

Q A first order reaction takes 30 Minutes for 50T .

completion calculate the time required for 90T com pl


.
. .

of this reaction

ARE tye 30 min

tyz 0¥93 k
063901 min
= =
g
-

tag
2.203T log
.
= a-
a x
-

&o3÷x3o log
=

go

99.7 min
dj3g÷gx3o log
= to = .

PseudoTuFirst0rdeoReactionmT
crew-wer

A reaction that appear to be of higher order but

follows first order kinetics under certain conditions


is called pseudo first order reaction .

"

In this type of reactions one of the

reactant is present in excess but other is present


small amount !
'
in

e.g Hydrolysis of ester


CH COO
, Cg Hs +
Hg O CHZCOOH tf tf - OH
(excess )

Rate K CCH COO


f Hs)
=
,

*
rate of these reactions depends upon the reactant
in lower concentration
present .

.CH#uctofCatal4stwT
wirer Those substance which
change
chemical Rxn without
the speed of a
undergoing
any change in itself
- Catalyst increase the rate of
reduced
rxh
by providing an alternate path with

activation energy .

Positive
mmmm
Catalyst
which increase the
speed of reaction

Negative
murmur
catalyst exegete

which decrease the


speed of reaction .

ftp.fdef

Q .

Ang .

cuz COOCH, t H2O cuz COOH + CH ou


,
for a Ist order Rxn .

2.3ft log cadge


K =
At t
-

- 605
0.02311

12=2.3%3 log off


s I
-

At E- 305,

K=
93%1 log since value of Kis
0.30
= 0.02311 s
- I constant for fist order
kinetics .
Q A first order reaction is tot .

complete in so minutes -

calculate the value of rate constant CK ) In what

time
,
the rxn be got .

completed
Any Acc . to first order kinetics

6.386×153
2.39¥ log {¥ 2-3%3-1 gtfo
K -
- or K - = mini

Time required for 90% Completion of the Rin


t =

£3,91 log too = 2.30L log to =


360.63 minutes .

6. 386×10-3

Q .
And let sale of this rxn

• =
KEN me
clash
then
ftp.go.kco-is-ho.sn K C O -

153M ( O 30)
-
h

z (Ith NTI
or -
-

Again
¥ %Igo=kGi5mh
-

307M 151N K CO -

co -

m
or
ta
=

(f) 1n=2I
expression for sale law
'
z= KEN
2 Ed ]
,

fig substituting the values in experiment 6.)


'
0.60 M min I K CO ISM )2 CO 15M)
-

-
= -

or
K = O .
60 = 177.77 M
-2 min -
I

70225×055

mi: :: me
:i::÷::÷÷fm]
iii. o
-
-
"

Gift All the Best


Q calculate the half life of
-

a first order
reactions from their rate constant given below .

lit doo s e
-

Cii , 2 min -
I Ciii ) 4 years I
-

n
And Ci ) Half life , tyz
0¥93 ¥93 3.465 X 10-3 see
-
-
= a .

iii Half life sty


0¥93 0£93 0.3465 Min
= =
. =

Mi's Half life ty,


0¥93 0*93=0-17325 Year
-
-
=
,

4- Thank You →

PKasemedotzg.
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pe#gBlharatPancnal-y
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