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Nitro compounds are considered as the derivaties of hydrocarbons. If one of the hydrogen atom of hydrocarbon is replaced by the -NO2 group, the resultant organic compound is called a nitrocompound.
Nitroalkanes are represented by the formula, R-NO2 where R is an alkyl group (CnH2n+1-) . Nitroalkanes are further classified into primary, secondary, tertiary nitroalkanes on the basis of type of carbon atom to which the nitro (-NO2) group is attached.
In the IUPAC nomenclature, the nitroalkanes are named by adding prefix nitro before the name of alkane, the position of the nitro group is indicated by number.
Nitroalkanes exhibit chain and position isomerism among their own class and functional isomerism with alkyl nitrites and special type tautomerism can also exist in nitro alkanes having an α-H atom. For example, nitro compounds having the molecular formula C4H9 NO2 exhibit the following isomerisms.
Tautomerism: Primary and secondary nitroalkanes, having α-H , also show an equilibrium mixture of two tautomers namely nitro – and aci – form
Tertiary nitro alkanes donot exhibit tautomerism due to absence of α-H atom.
• Less acidic
• Dissolves in NaOH slowly
• Decolourises FeCl3 solution
• Electrical conductivity is low
Aci – form
• More acidic
• Dissolves in NaOH instantly
• With FeCl3 gives reddish brown colour
• Electrical conductivity is high
The α-H atom of 1 & 2 nitroalkanes show acidic character because of the electron with drawing effect of NO2 group. These are more acidic than aldehydes, ketones, ester and cyanides. Nitroalkanes dissolve in NaOH solution to form a salt. Aci – nitro derivatives are more acidic than nitro form. When the number of alkyl group attached to α carbon increases, acidity decreases. due to +I effect of alkyl groups.
Write all possible isomers for the following compounds.
i) C2 H5 -NO2 ii) C3 H7 -NO2
a) Alkyl bromides (or) iodides on heating with ethanolic solution of potassium nitrite gives nitroethane.
The reaction follows SN2 mechanism.
This method is not suitable for preparing nitrobenzene because the bromine directly attached to the benzene ring cannot be cleaved easily.
Gaseous mixture of methane and nitric acid passed through a red hot metal tube to give nitromethane.
Except methane, other alkanes (upto n – hexane) give a mixture of nitroalkanes due to C-C cleavage. The individual nitro alkanes can be separated by fractional distillation.
α- choloroacetic acid when boiled with aqueous solution of sodium nitrite gives nitromethane.
Find out the product of the following reactions.
tert – butyl amine is oxidised with aqueous KMnO4 to give tert – nitro alkanes.
Oxidation of acetaldoxime and acetoneoxime with trifluoroperoxy acetic acid gives nitroethane (1º) and 2 – nitropropane (2 º) respectively.
When benzene is heated at 330K with a nitrating mixture (Con.HNO3 + Con.H2SO4 ) , electrophilic substitution takes place to form nitro benzene. (Oil of mirbane)
On direct nitration of nitrobenzene m- dinitrobenzene is obtained
Nitration of nitro benzene gives m-dinitrobenzene. The following method is adopted for the preparation of p-dinitrobenzene.
Amino group can be directly converted into nitro group, using caro’s acid (H2 SO5) (or) persulphuric acid (H2 S2O8 ) (or) peroxytrifluro acetic acid (F3 C.CO3H) as oxidising agent.
The lower nitroalkanes are colourless pleasant smelling liquids, sparingly soluble in water, but readily soluble in organic solvents like benzene, acetone etc… They have high boiling points because of their highly polar nature. Alkylnitrites have lower boiling points than nitro alkanes.
Nitroalkanes undergo the following common reactions.
i. Reduction ii. Hydrolysis iii. Halogenations
Reduction of nitroalkanes has important synthetic applications. The various reduction stages of nitro group are given below.
The final product depends upon the nature of reducing agent as well as the pH of the medium.
Ethylnitrite on reduction with Sn / HCl gives ethanol
Hydrolysis can be effected using conc. HCl or conc. H2SO4 . Primary nitroalkanes on hydrolysis gives carboxylic acid, and the secondary nitroalkanes give ketones. The tertiary nitroalkanes have no reaction.
On the other hand, the acid or base hydrolysis of ethyl nitrite gives ethanol.
iii. Halogenation of nitroalkanes
Primary and secondary nitroalkanes on treatement with Cl2 or Br2 in the presence of NaOH give halonitroalkanes. The α - H atom of nitroalkanes are successively replaced by halogen atoms.
Nitroethane is suspected to cause genetic damage and be harmful to the nervous system.
iv. Nef carbonyl synthesis :
Nitrobenzene reduction with Ni (or) Pt, (or) LiAlH4 to give aniline
Selective reduction of polynitro compounds
The electrophilic substitution reactions of nitrobenzene are usually very slow and vigorous reaction condition have to be employed (- NO2 group is stongly deactivating and m – directing).
Nitrobenzene does not undergo Friedel – Crafts reactions due to the strong deactivating nature of -NO2 group.
Predict the major product that would be obtained on nitration of the following compounds
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