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:
Write the IUPAC names of the following ketones and aldehydes. Wherever possible, give also common names. \((i) CH_3CO(CH_2)_4CH_3 \)\((ii) CH_3CH_2CHBrCH_2CH(CH_3)CHO \)\((iii) CH_3(CH_2)_5CHO \)\((iv) Ph-CH=CH-CHO\)\((v)\)\((vi) PhCOPh\)
You are given benzene,conc.H2SO4 and NaOH.Write the equations for the preparation of phenol using these reagents.