Answer
Verified
374.7k+ views
Hint: Nitrosyl chloride is a chemical compound with molecular formula $ NOCl $ . It is a yellow gas which is commonly termed as a component of aqua regia i.e., a mixture of nitric acid and hydrochloric acid. It is widely used in organic reactions due to its strong electrophilic and oxidizing nature. It is also known as Tilden’s reagent.
Complete answer:
The addition of nitrosyl chloride to an ethene molecule takes place in three steps. The mechanism for the addition reaction of $ NOCl $ to ethene is as follows:
Step-1: Dissociation of nitrosyl chloride into respective cation and anion. The reaction takes place as follows:
$ NOCl \rightleftharpoons N{O^ + } + C{l^ - } $
Step-2: In ethene, $ s{p^2} $ hybridized carbon is electronegative in nature i.e., it consists of an electron rich carbon atom which attacks the nitrosonium ion and formation of carbocation will take place as an intermediate. The reaction proceeds as follows:
Step-3: The chloride ion will act as a nucleophile and attack the carbocation formed in the previous step to give the final product. The reaction proceeds as follows:
Hence, the final diagram for the given reaction mechanism will be as follows:
Note:
It is important to note that the addition of nitrosyl chloride to ethene is a stereospecific reaction i.e., the two stereochemical products are possible after the reaction. If chloride ion attacks carbocation from the sample plane where the nitrosyl group is attached, then the product formed is syn whereas if chloride ion attacks from opposite plane, then the product formed is termed as anti.
Complete answer:
The addition of nitrosyl chloride to an ethene molecule takes place in three steps. The mechanism for the addition reaction of $ NOCl $ to ethene is as follows:
Step-1: Dissociation of nitrosyl chloride into respective cation and anion. The reaction takes place as follows:
$ NOCl \rightleftharpoons N{O^ + } + C{l^ - } $
Step-2: In ethene, $ s{p^2} $ hybridized carbon is electronegative in nature i.e., it consists of an electron rich carbon atom which attacks the nitrosonium ion and formation of carbocation will take place as an intermediate. The reaction proceeds as follows:
Step-3: The chloride ion will act as a nucleophile and attack the carbocation formed in the previous step to give the final product. The reaction proceeds as follows:
Hence, the final diagram for the given reaction mechanism will be as follows:
Note:
It is important to note that the addition of nitrosyl chloride to ethene is a stereospecific reaction i.e., the two stereochemical products are possible after the reaction. If chloride ion attacks carbocation from the sample plane where the nitrosyl group is attached, then the product formed is syn whereas if chloride ion attacks from opposite plane, then the product formed is termed as anti.
Recently Updated Pages
what is the correct chronological order of the following class 10 social science CBSE
Which of the following was not the actual cause for class 10 social science CBSE
Which of the following statements is not correct A class 10 social science CBSE
Which of the following leaders was not present in the class 10 social science CBSE
Garampani Sanctuary is located at A Diphu Assam B Gangtok class 10 social science CBSE
Which one of the following places is not covered by class 10 social science CBSE
Trending doubts
Which are the Top 10 Largest Countries of the World?
How do you graph the function fx 4x class 9 maths CBSE
Fill the blanks with the suitable prepositions 1 The class 9 english CBSE
The only snake that builds a nest is a Krait b King class 11 biology CBSE
The Equation xxx + 2 is Satisfied when x is Equal to Class 10 Maths
In Indian rupees 1 trillion is equal to how many c class 8 maths CBSE
Give 10 examples for herbs , shrubs , climbers , creepers
Why is there a time difference of about 5 hours between class 10 social science CBSE
Which places in India experience sunrise first and class 9 social science CBSE