How will you prepare the following compounds from benzene?You may use any inorganic reagent and any organic reagent having not more than one carbon atom(i)Methyl benzoate (ii) m-Nitrobenzoic acid (iii)p-Nitrobenzoic acid (iv)Phenylacetic acid (v)p-Nitrobenzaldehyde.
Mention the factors that affect the rate of a chemical reaction.
The decomposition of dimethyl ether leads to the formation of CH4, H2 and CO and the reaction rate is given by \(Rate = k [CH_3OCH_3]^{\frac 32}\)The rate of reaction is followed by increase in pressure in a closed vessel, so the rate can also be expressed in terms of the partial pressure of dimethyl ether, i.e., \(Rate = k(p_{CH_3OCH_3})^{\frac 32}\)If the pressure is measured in bar and time in minutes, then what are the units of rate and rate constants?
The decomposition of NH3 on platinum surface is zero order reaction. What are the rates of production of N2 and H2 if k = 2.5 x 10-4 mol-1Ls-1?
For the reaction:\(2A + B → A_2B\)the rate = k[A][B]2 with k= 2.0 x 10-6 mol-2L2s-1. Calculate the initial rate of the reaction when [A] = 0.1 mol L-1, [B] = 0.2 mol L-1. Calculate the rate of reaction after [A] is reduced to 0.06 mol L-1.
From the rate expression for the following reactions, determine their order of reaction and the dimensions of the rate constants.
An organic compound(A)(molecular formula\( C_8H_{16}O_2\))was hydrolysed with dilute sulphuric acid to give a carboxylic acid(B)and an alcohol(C).Oxidation of(C)with chromic acid produced (B).(C)on dehydration gives \(but-1-ene\).Write equations for the reactions involved.
Write structural formulas and names of four possible aldol condensation products from propanal and butanal.In each case,indicate which aldehyde acts as nucleophile and which as electrophile.
Write down the IUPAC name for each of the following complexes and indicate the oxidation state, electronic configuration and coordination number. Also give stereochemistry and magnetic moment of the complex:\((i) K[Cr(H_2O)_2(C_2O_4)_2].3H_2O\)\((ii)[Co(NH_3)_5Cl]Cl_2\)\((iii) CrCl_3(py)_3\)\((iv) Cs[FeCl_4]\)\((v)K_4[Mn(CN)_6]\)
Draw structures of the following derivatives. (i)The 2,4-dinitrophenylhydrazone of benzaldehyde (ii)Cyclopropanone oxime (iii)Acetaldehydedimethylacetal (iv)The semicarbazone of cyclobutanone (v)The ethylene ketal of hexan-3-one (vi)The methyl hemiacetal of formaldehyde
Give equations of the following reactions:(i)Oxidation of propane-1-ol with alkaline KMnO4 solution.(ii)Bromine in CS2 with phenol.(iii)Dilute HNO3 with phenol.(iv)Treating phenol with chloroform in the presence of aqueous NaOH
Explain how does the –OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?
Give two reactions that show the acidic nature of phenol. Compare the acidity of phenol with that of ethanol.The acidic nature of phenol can be represented by the following two reactions: