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Write the order of reactivity of alkyl halides with ammonia. - Chemistry

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प्रश्न

Write the order of reactivity of alkyl halides with ammonia.

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उत्तर

The order of reactivity of alkyl halides with ammonia is, R–I > R–Br > R–Cl.

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अध्याय 13: Amines - Very Short Answer Questions

संबंधित प्रश्न

How is ethyl amine prepared from methyl iodide?


Identify the compounds 'A' and 'B' in the following equation:


How do you convert the following: C6H5CONH2 to C6H5NH2


Give the structures of A, B and C in the following reactions :


Write a short note on the following:

Hoffmann’s bromamide reaction


Accomplish the following conversion:

Nitrobenzene to benzoic acid


Give the structure of A, B and C in the following reaction:

\[\ce{CH3CH2I ->[NaCN] A ->[OH-][Partial hydrolysis] B ->[NaOH + Br2] C}\]


Give the structure of A, B and C in the following reaction:

\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]


Give the structure of A, B and C in the following reaction:

\[\ce{C6H5NO2 ->[Fe/HCl] A ->[NaNO2 + HCl][273 K] B ->[H2O/H+][\Delta] C}\]


Give the structures of A, B and C in the following reaction:

\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]


Write the reaction of aromatic primary amine with nitrous acid.


Give a plausible explanation for the following:

Why are amines less acidic than alcohols of comparable molecular masses?


Arrange the following in the increasing order of their pKvalues:

C6H5NH2, C2H5NH2, C6H5NHCH3


Give the structures of A, B and C in the following reactions :


Write reactions to prepare ethanamine from Acetonitrile.


Name the process of breaking C-X bond by ammonia in preparation of amines.


Write reactions to bring about the following conversions.

Acetamide to methylamine


Alkyl cyanides on reduction by sodium and ethanol give primary amines. This reaction is called as ____________.


The end product C of the following reaction is

\[\ce{C2H5NH2 ->[HNO2] A ->[PCl5] B ->[NH3][Alcohol] C}\]


Identify the product obtained, when benzamide is treated with bromine and aqueous sodium hydroxide.


____________ can be prepared exclusively by Gabriel phthalimide synthesis.


What product is formed when \[\ce{R - C ≡ N}\] is hydrolysed?


\[\ce{CH3-CN ->[Na/C2H5OH]}\]

The product formed is ____________.


Which nitrogen containing compound amongst the following would undergo Mendius reduction to furnish primary amine \[\ce{(R - NH2)}\]?


Which of the following amines forms a clear solution when treated with benzene sulphonyl chloride and excess of potassium hydroxide?


Identify the INCORRECT statement regarding Hofmann bromamide reaction.


Which of the following amines cannot be prepared by Gabriel phthalimide synthesis?


Which of the following reagents is used in Hofmann's elimination reaction of amines?


For producing amines, the reaction of nitro compounds with iron scrap is preferred because:


Benzylamine may be alkylated as shown in the following equation:

\[\ce{C6H5CH2NH2 + R - X -> C6H5CH2NHR}\]

Which of the following alkylhalides is best suited for this reaction through SN1 mechanism?


The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is ______.


The best reagent for converting, 2-phenylpropanamide into 1- phenylethanamine is ______.


Hoffmann Bromamide Degradation reaction is shown by ______.


Best method for preparing primary amines from alkyl halides without changing the number of carbon atoms in the chain is ______.


Which of the following compounds is the weakest Brönsted base?


Which of the following reactions are correct?

(i)

(ii)

(iii)

(iv)


Under which of the following reaction conditions, aniline gives p-nitro derivative as the major product?

(i) Acetyl chloride/pyridine followed by reaction with conc.\[\ce{H2SO4 }\] + conc. \[\ce{HNO3}\].

(ii) Acetic anyhdride/pyridine followed by conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].

(iii) Dil. HCl followed by reaction with conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].

(iv) Reaction with conc.\[\ce{HNO3}\] + conc.\[\ce{H2 SO4}\].


Write following conversions:

nitrobenzene `->` acetanilide


How will you bring out the following conversion?


Assertion: Hoffmann’s bromamide reaction is given by primary amines.

Reason: Primary amines are more basic than secondary amines.


Account for the following:

Aniline cannot be prepared by the ammonolysis of chlorobenzene under normal conditions.


A primary amine is formed by an amide on treatment with bromine and alkali. The primary amine has


The compound X is which of the following?

\[\ce{CH3CN ->[Na + C2H5OH] x}\]


Reduction of nitro alkanes yields which compound?


In the given reaction what is the X?

\[\begin{array}{cc}
\ce{O}\phantom{.......................}\\
||\phantom{.......................}\\
\phantom{}\ce{R - C - OH <-[H3O] Χ ->[H] RCH2NH2}
\end{array}\]


Which of the following compound is expected to be most basic?


C6H5CONHCH3 can be converted into C6H5CH2NHCH3 by:-


When primary amines are treated with HCl, the product obtained is which of the following?


Which of the following CANNOT be prepared by ammonolysis of alkyl halide?


Methyl amine on reaction with chloroform in the presence of NaOH gives ______.


Amides can be converted into amines by the reaction named ______.


Write short note on the following.

Ammonolysis.


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