(i) PhMgBr and then H3O+: CH3CH2CH(OH)Ph (1-phenylpropan-1-ol). (ii) LiAlH4: CH3CH2CH2OH (propan-1-ol). (iii) HCN: CH3CH2CH(OH)CN (2-hydroxybutanenitrile).
Molar conductivity is the conducting power of all the ions produced by dissolving one mole of an electrolyte in a solution. It is defined as κ/c. It increases with decrease in concentration because the total volume of solution containing one mole of electrolyte increases, leading to an increase in the degree of dissociation and mobility of ions.
Average Rate = -1/2 * (Δ[N2O5]/Δt) = -1/2 * (0.4 - 0.5)/10 = 0.005 mol L^-1 min^-1. Rate of production of NO2 = 4 * Rate of reaction (using stoichiometry) = 4 * (Rate of -1/2 * Δ[N2O5]/Δt) = 2 * (0.1/10) = 0.02 mol L^-1 min^-1.
(i) Due to their ability to adopt multiple oxidation states and form complexes, providing a large surface area for reactants to adsorb. (ii) They have completely filled d-orbitals (d10) in their ground state and excited state. (iii) Due to the lanthanoid contraction, which offsets the expected increase in atomic size.
(i) Due to the extra stability of the half-filled d5 configuration in Mn2+. (ii) Irregularities arise due to varying trends in first and second ionization enthalpies along with sublimation and hydration energies. (iii) Because the high energy required to transform Cu(s) to Cu2+(aq) is not compensated by its hydration enthalpy.
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Log in to view solution →Amines constitute an important class of organic compounds derived by replacing one or more hydrogen atoms of ammonia molecule by alkyl/aryl groups. Amines are usually formed from nitro compounds, halides, amides, etc. They exhibit hydrogen bonding which influences their physical properties. Alkyl amines are found to be stronger bases than ammonia. In aromatic amines, electron releasing and withdrawing groups, respectively increase and decrease their basic character. Reactions of amines are governed by availability of the unshared pair of electrons on nitrogen. Influence of the number of hydrogen atoms at nitrogen atom on the type of reactions and nature of products is responsible for identification and distinction between primary, secondary and tertiary amines. Reactivity of aromatic amines can be controlled by acylation process.
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