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Tertiary Butyl Nitrite Triggered Nitration of Phenols: Solvent‐ and Structure‐Dependent Kinetic Study
Author(s) -
Kumar M. Satish,
Rajanna K. C.,
Venkateswarlu M.,
Rao K. Lakshman
Publication year - 2016
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/kin.20979
Subject(s) - chemistry , nitration , acetonitrile , solvent , solvent effects , reaction rate constant , hammett equation , reactivity (psychology) , phenols , formamide , solvation , nitrite , toluene , kinetics , computational chemistry , organic chemistry , nitrate , medicine , physics , alternative medicine , pathology , quantum mechanics
Nitration of phenols with tertiary butyl nitrite (TBN) obeyed second‐order kinetics with a first‐order dependence on [TBN] and [phenol] under acid‐free conditions. Reaction rates were significantly altered by a change in the dielectric constant and other physical properties of solvent. The rate of nitration increased with an increase in temperature (303–323 K) in different solvent media (acetonitrile, dichloroethane, CCl 4 , dimethyl formamide (DMF), and toluene). The rates of nitration (log k ) could not fit into either Amis or Kirkwood plots [log k ’ vs. (1/ D ) or [( D – 1)/(2 D + 1)], but the trends were better explained by the basic form of multivariate linear solvent energy relationships (MLSER) suggested by the Koppel and Palm approach on the one hand and the Kamlet and Taft approach on the other hand. These observations probably substantiate that cumulative contributions of basic solvent parameters (equilibrium as well as frictional solvent effects) and solvent–solute interactions for solvation of transition state during nitration of phenols. Reaction rates accelerated with the introduction of electron‐donating groups and retarded with electron‐withdrawing groups. Accordingly, the reactivity of structurally different phenols was found to follow the following sequence: p ‐OH > p ‐MeO > p ‐Me > H > m ‐Me > p ‐Cl > p‐ Br > m ‐Cl > p ‐NO 2 > m ‐OH. The results are interpreted by Hammett's theory of linear free energy relationship. The reaction constant (Hammett's ρ) is a measure of the sensitivity of the reaction toward the electronic effects of the substituent. The rho (ρ) values obtained from the present experiments are fairly large negative values (ρ < 0), indicating attack of an electrophile on the aromatic ring. An increase in temperature decreases the reaction constant (ρ) values. According to Exner, ρ values for a given reaction are influenced by the temperature according to the following relation: ρ = A [1 – β / T ]. Obtained “isokinetic temperature ( β )” values are in the range of 225–290. These values are far below the experimental temperature range (303–323 K), indicating that the entropy factors are probably more important in controlling the reaction. This point can be seen from the negative entropy values and linearity of multiple linear regression analysis (MLRA). Furthermore, in the present study, rate constants for TBN nitration of ortho‐substituted phenols could not fit into Taft's plots of log( k / k CH3 ) versus σ* or, E s or combined Taft's relationship. However, Charton's MLRA of the log k with polar, resonance, steric, hydrophobicity, and molar refractivity showing a very good linear relationship was obtained. It is of interest to note that when log k exp values are correlated with log k cal a perfect linearity is obtained with a correlation coefficient of unity, indicating the consonance between experimental and calculated rate constants in the present work.