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= =
2
1
2
zke
TE
r
=
5
19. Velocity of e No
. Of revolution in 1 sec
6
2.188 10 2
/ m s
n
2
16
3
1.326 10
2
V z
rn n
=
20. Debroglie
( )
; .
2 2 .
h h h h
mv p meV m K E
= = = =
21. Frequency of matter wave =
2
2 V mv KE
h h
= =
22. Heisenburg ( ) ( )
4
h
x m v
23.
0
KE hv hv =
0
v - Threshold frequency
24. Schrodinger
3/ 2
2 2
3 2
0 0
1 1 18 2
27
3 81 3
s
r r
e
a ao ao a
| | | |
= +
| |
\ \
Has node at
0
r r = Find ( )
0 0
r f a =
-concept of Nodes, Nodal Planes
25. ( ) H H n RT = + at const P
H E = at const vol.
Its always products reactants except when HL & BDE are used
f
H = ( ) ( )
C
H react Hc prod
Hc =
f
H (products) -
f
H (Reactants)
G H T S =
0
2.303 log G G RT Q = +
Criterion for spontaneity
26. Relation between
p c
K and K
p c
p c
p c
K K
K K
K K
=
<
>
for which reaction
27. Units of &
p c
K K
28. Calculation of
p c
K and K in altered reaction
29. Characteristics of equilibrium
30.
sp
K in cells -
x y
A B
31. PH PH of buffer PH of weak electrolytes very dil
( )
8
10
6
32.
h
K C
2
( = degree of hydrolysis)
33. Theories Bronsted Lowry, Lewis
34. Faradays Laws (1F = 96,500 columbs = 1 mole of 1 e
=
35. Production of Electrolysis State (molton v/s aq)
Electrode (passive v/s active)
Conc. (50%
2 4 2 4
/ H SO v s dil H SO )
36. E.M.F Nemst
n
sp
Eq K conc. Cells
-After electrolysis from
0 0
G nFE =
37. Order
38. Arhenius Temp
39. Parallel path decay
40. Half life carbon dating
41. Cell edge diagonal volume density No of atoms
42. Raoults law
43. Isotonicity Vant Hoffs factor association dissociation
44. Physical v/s chemical adsorption
45. Factors affecting adsorption
46. Micell Emulsifying agent ; Lyophilic Lyophobic paratial size
47. Peptization v/s Flocculation Hardy schulz Rule
48. CMC
49. ; ,
N
P
- decay
50. Radio active equilibrium Sr; Rb ratio type
ORGANIC CHEMISTRY
1. Stability due to resonance Hyper conjugation
2. Geometric No free rotation trans more stable than cis
-dipole moment of trans = O
3. Dipeptide in
NH
2
COOH
NH
2
+
HOOC COOH
NH
2
4. Optical MeSO, Racemic, diasteromers, enantiomers
5. Conformation of ethane, butane stability, type of strain
Reason free rotation
7
6. Keto enol Tautomerism more when EWG present
7. Effect + I, -I, +M, -M
8. Orientation in Benzene
9. Acidity of R-COOH conjugate stability If necessary
10. Basicity of Amine conjugate stability If necessary
11. Stability of carbocation
12. Wurtz, decarboxylation free radical
13. Addition to C = C Morkownikov kharasch
- Stability of intermediate
-carbocation
-rearrangement
14. Pinacol Pinacolone (with ring expansion)
15. Elimination Zaisev, - more substituted
Hoffmann Less substituted
16. Ozonolysis
17.
2
2 2
water
Hg
C H
+
&
Re
Cu Ag
d White
PPT PPT
18. Aromaticity
19. Orientation in subst. Bnezenes (disubstitute)
20.
1 2
SN and SN
21. Aldol & cannizaro, HVZ Esterification
22. Nitrobenzene
Reduction
23. Diazotisation coupling
24. Glucoses, fructose Reduction ( )
3 2 2
, HNO Br H O +
25. Hydrolysis of sugar
26. Mutarotation
27. Zwitter ion
28. Polymers
29. Lassaignes Test Results
30. Hoffmann Bromamide
31. Carbyl amine Test
32. Chloroform
33. Beck Man Rearrangement