
How will you obtain ethyl isothiocyanate from ethylamine $ ? $
Answer
503.4k+ views
Hint :We can obtain ethyl isothiocyanate from ethylamine by four methods. First, by treating ethyl amine and chloroform with potassium hydroxide, by pyrolyzing the complex between ethyl isothiocyanate and triethyl phosphine and lastly, by passing ethylene and hydrogen cyanide through an electric discharge.
Complete Step By Step Answer:
$-$ We can obtain isothiocyanate by treating ethyl amine and chloroform with potassium hydroxide.
The carbylamine reaction is the synthesis of an isocyanide by the reaction of a primary amine, chloroform, and base. The conversion involves the intermediacy of dichlorocarbene. It is used to prepare secondary amines.
When heated with chloroform and ethanolic potassium hydroxide, form foul-smelling isocyanides or carbylamines.
$-$ We can obtain isothiocyanate by pyrolyzing the complex between ethyl isothiocyanate and triethyl phosphine.
$-$ Also, by heating cyanocobal tic acid with ethanol.
$-$ And lastly, by passing ethylene and hydrogen cyanide through an electric discharge.
Ethylene and hydrogen cyanide was passed through these discharge tubes at a constant velocity for the period of the reaction. Two moles of hydrogen cyanide are used. A current of $ 60 $ cycles was sent through a voltage regulator.
Note :
Remember during the pyrolysis sometimes the liquid crystallizes to a dense solid which immobilizes the stirrer if it has not been raised. The crystallization has no effect on subsequent steps except to necessitate a longer period of stirring after the potassium cyanide is added. Also, the aqueous cyanide solution can be disposed of by flushing it down the drain with a large volume of water and it is very toxic.
Complete Step By Step Answer:
$-$ We can obtain isothiocyanate by treating ethyl amine and chloroform with potassium hydroxide.
The carbylamine reaction is the synthesis of an isocyanide by the reaction of a primary amine, chloroform, and base. The conversion involves the intermediacy of dichlorocarbene. It is used to prepare secondary amines.
When heated with chloroform and ethanolic potassium hydroxide, form foul-smelling isocyanides or carbylamines.
$-$ We can obtain isothiocyanate by pyrolyzing the complex between ethyl isothiocyanate and triethyl phosphine.
$-$ Also, by heating cyanocobal tic acid with ethanol.
$-$ And lastly, by passing ethylene and hydrogen cyanide through an electric discharge.
Ethylene and hydrogen cyanide was passed through these discharge tubes at a constant velocity for the period of the reaction. Two moles of hydrogen cyanide are used. A current of $ 60 $ cycles was sent through a voltage regulator.
Note :
Remember during the pyrolysis sometimes the liquid crystallizes to a dense solid which immobilizes the stirrer if it has not been raised. The crystallization has no effect on subsequent steps except to necessitate a longer period of stirring after the potassium cyanide is added. Also, the aqueous cyanide solution can be disposed of by flushing it down the drain with a large volume of water and it is very toxic.
Recently Updated Pages
Why are manures considered better than fertilizers class 11 biology CBSE

Find the coordinates of the midpoint of the line segment class 11 maths CBSE

Distinguish between static friction limiting friction class 11 physics CBSE

The Chairman of the constituent Assembly was A Jawaharlal class 11 social science CBSE

The first National Commission on Labour NCL submitted class 11 social science CBSE

Number of all subshell of n + l 7 is A 4 B 5 C 6 D class 11 chemistry CBSE

Trending doubts
Differentiate between an exothermic and an endothermic class 11 chemistry CBSE

10 examples of friction in our daily life

One Metric ton is equal to kg A 10000 B 1000 C 100 class 11 physics CBSE

Difference Between Prokaryotic Cells and Eukaryotic Cells

1 Quintal is equal to a 110 kg b 10 kg c 100kg d 1000 class 11 physics CBSE

State the laws of reflection of light

