Chemistry
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New answer posted
a year agoContributor-Level 10
This is a short answer type question as classified in NCERT Exemplar
Due to the +R effect halogens are ortho and para directing groups.

New answer posted
a year agoContributor-Level 10
The electrons may be assigned to the following orbitals :
(i) 4d
(ii) 3d
(iii) 4p
(iv) 3d
(v) 3p
(vi) 4p.
The increasing order of energy is :
(v) < (ii) = (iv) < (vi) = (iii) < (i)
New answer posted
a year agoContributor-Level 10

Since actual momentum is smaller than the uncertainty in measuring momentum, therefore, the momentum of electron cannot be defined
New answer posted
a year agoContributor-Level 10
This is a short answer type question as classified in NCERT Exemplar
The electron donating group increases the reactivity in electrophilic substitution reaction whereas the electron withdrawing group decreases the reactivity in electrophilic substitution.
Thus, the order of reactivity

New answer posted
a year agoContributor-Level 10
ν = 4.37 x 105 m s-1, m = 0.1 kg
As per de Brogile's equation,
λ= m/v = (6.626 x 10-34 kg m2 s-1) / (0.1 kg) x (4.37 x 105 m s-1)
=6.626/0.437 x 10-34-5 m
= 1.516 x 10-38 m
New question posted
a year agoNew answer posted
a year agoContributor-Level 10
This is a short answer type question as classified in NCERT Exemplar

New answer posted
a year agoContributor-Level 10
ν = 2.19 x 106 m s-1
As per de Brogile's equation,
λ= m/v = (6.626 x 10-34 kg m2 s-1) / (9.1 x 10-31 kg) x (2.19 x 106 m s-1)
6.626/91 * 2.19= x 10-34+25 m = 0.33243 x 10-9 m = 332.43 pm
New answer posted
a year agoContributor-Level 10
λ = 800 pm = 800 x 10-12 m
m = 1.675 x 10-27 kg
As per de Brogile's equation,
ν =h/mλ = (6.626 x 10-34 kg m2 s-1) / (1.675 x 10-27 kg) x (800 x 10-12 m)
=6.626/1.675 * 8 x 10-34+27+10
= 0.494 x 103 ms-1
= 494 ms-1
New answer posted
a year agoContributor-Level 10
This is a short answer type question as classified in NCERT Exemplar
The benzene here would undergo Friedel-Crafts alkylation reaction where carbocation is formed as an intermediate, thus secondary carbocation is formed as an intermediate due to its greater stability than that of the primary carbocation.
The final product obtained is

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