Answer:
None of these
Explanation:
Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.
Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :
Step -1 : Generation of stable carbocation.
Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.
Step-2: Attack of the ring to the carbocation
The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.
The product formed is shown in mechanism does not mention in any of the options.
So, None of these is the answer
Explanation:
The given data is as follows.
Refractive index of mixture = 1.456
Refractive index of hexane = 1.375
Refractive index of toulene = 1.497
Let mole fraction of hexane =
and, mole fraction of toulene =
Also,
or,
Hence, calculate the mole fraction of hexane as follows.
refractive index mixture= mole fraction hexane × ref index hexane + mole fraction toluene × ref index toluene.
1.456 =
1.456 =
0.081 =
=
= 0.66
Since,
= 1 - 0.66
= 0.34
Thus, we can conclude that mole fraction of hexane in your sample is 0.34.
I think B qualitative is the answer