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First Step: Friedel Craft Acylation on benzene to form phenyl methyl ketone or acetophenone.
Second Step: Reduction of acetophenone by Clemmenen reduction using zinc amalgam and HCl to give the desired product. Another method is the reaction of benzene with ethyl chloride in presence of AlCl3 and heat in a close container.
What else can I help you with?
Why methyl aclcohol soluble in water and benzene is not?
The solubility difference between methyl alcohol (CH3OH) and benzene (C6H6) is related to the polar nature of methyl alcohol and the non polar nature of benzene. The OH group on methyl alcohol makes this a polar molecule and thus soluble in water. The lack of such a polar group in benzene makes it non polar, and thus insoluble in water.
What is the group difference between toluene and benzene?
Benzene - a six carbon, six hydrogen [planar] ring - C6H6 - has no side-groups. Yet when any one single side-hydrogen is replaced with one Methyl (-CH3) Group, we have Toluene. Short Answer = one methyl group.
What is the formation formula of methyl benzene?
The formula for methylbenzene, also known as toluene, is C7H8. It consists of a benzene ring with a methyl group (-CH3) attached to it.
Why methyl attached to benzene is ortho-para director group?
This group attached to benzene ring acts as the ortho-para directing group due to Hyperconjugation.
Which isomer of xylene does form only one trisubstituted benzene?
1,3-dimethylbenzene (meta-xylene) forms only one trisubstituted benzene due to its symmetrical structure, where the two methyl groups are in the meta positions with respect to each other on the benzene ring. This symmetry allows for only one possible trisubstituted product to form.
What separation method do you use to separate benzene from a mixture of benzene and methyl benzene?
Fractional distillation is commonly used to separate benzene from a mixture of benzene and methyl benzene. Benzene has a lower boiling point compared to methyl benzene, allowing it to be separated by distillation based on the difference in their boiling points.
Does toluene contain benzene?
toluene is the name for methyl benzene. You have a benzene ring of C6H6 . One of the hydrogens (H) is substituted for a methyl functional group Hence its structure is C6H5-CH3
What is the chemical formula for methyl benzene?
The chemical formula for methyl benzene, also known as toluene, is C7H8.
Why methyl aclcohol soluble in water and benzene is not?
The solubility difference between methyl alcohol (CH3OH) and benzene (C6H6) is related to the polar nature of methyl alcohol and the non polar nature of benzene. The OH group on methyl alcohol makes this a polar molecule and thus soluble in water. The lack of such a polar group in benzene makes it non polar, and thus insoluble in water.
What is reactions of methyl benzene with iron powder?
burr
What is the group difference between toluene and benzene?
Benzene - a six carbon, six hydrogen [planar] ring - C6H6 - has no side-groups. Yet when any one single side-hydrogen is replaced with one Methyl (-CH3) Group, we have Toluene. Short Answer = one methyl group.
What is the formation formula of methyl benzene?
The formula for methylbenzene, also known as toluene, is C7H8. It consists of a benzene ring with a methyl group (-CH3) attached to it.
What is the chemical formula for keryl benzene?
The chemical formula for keryl benzene is C6H5CH3. It is a type of alkylated benzene where a methyl group is attached to the benzene ring.
What is additive in fuel?
Some additives I know of Ethyl methyl lead (octane booster and upper cylinder lube) Methyl Benzene (octane booster)
What happens when hydrochloride in dry form is dissolved in methyl benzene?
pH less than 7
What properties does benzene have to make it good to use?
Convert the benzene into Phenol which is a good antiseptic material.
How do you convert benzene to toluene?
Toluene + HNO3/H2SO4 --> p-nitrotoluene (para directed nitration) p-nitrotoluene + Zn/HCl --> p-aminotoluene (changing NO2 to NH2 by reduction) p-aminotoluene +Br2 --> bromination ortho to NH2 Remove NH2 via diazonium salt and decomposition with 1) HONO (which is NaNO2+HCl), 2) H3PO2 for the final product.
