Mention the conditions required to maximise the yield of ammonia.
Ammonia is prepared using the Haber’s process.
The conditions required to maximize the yield of ammonia are as follows:
1 In accordance to Le Chatelier’s principle ,low temperature will shift the equilibrium to the right because the reaction is exothermic.This gives greater yield of ammonia.Therefore a temperature of about 450°C will be optimal for the preparation of ammonia.
2 High pressure on the reaction at equilibrium favours the shift of the equilibrium to the right because the forward reaction proceeds with a decrease in number of moles.Hence a pressure of about 200 atm will be optimal for the higher yield of ammonia.
3 A catalyst should be used to increase the rate of reaction & to quickly attain equilibrium.For eg as iron oxide mixed with small amounts of K2O and Al2O3 can be used as catalyst.
4 N2 & H2 gases should be pure in nature to increase the yield of ammonia.
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Why are pentahalides more covalent than trihalides?
Give the formula and describe the structure of a noble gas species which is isostructural with:
(i) ICl-4
(ii) IBr-2
(iii) BrO-3
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How is O3 estimated quantitatively?
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(i) F2, Cl2, Br2, I2- increasing bond dissociation enthalpy.
(ii) HF, HCl, HBr, HI - increasing acid strength.
(iii) NH3, PH3, AsH3, SbH3, BiH3- increasing base strength.
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For the reaction R → P, the concentration of a reactant changes from 0.03 M to 0.02 M in 25 minutes. Calculate the average rate of reaction using units of time both in minutes and seconds.
Write the formulas for the following coordination compounds:
(i) Tetraamminediaquacobalt (III) chloride
(ii) Potassium tetracyanonickelate(II)
(iii) Tris(ethane-1,2-diamine) chromium(III) chloride
(iv) Amminebromidochloridonitrito-N-platinate(II)
(v) Dichloridobis(ethane-1,2-diamine)platinum(IV) nitrate
(vi) Iron(III) hexacyanoferrate(II)
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(ii) Write IUPAC names of all the isomers.
(iii) What type of isomerism is exhibited by different pairs of amines?
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Write the structures of the following compounds.
(i) α-Methoxypropionaldehyde
(ii) 3-Hydroxybutanal
(iii) 2-Hydroxycyclopentane carbaldehyde
(iv) 4-Oxopentanal
(v) Di-sec-butyl ketone
(vi) 4-Fluoroacetophenone
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Write structures of the following compounds:
(i) 2-Chloro-3-methylpentane
(ii) 1-Chloro-4-ethylcyclohexane
(iii) 4-tert. Butyl-3-iodoheptane
(iv) 1,4-Dibromobut-2-ene
(v) 1-Bromo-4-sec. butyl-2-methylbenzene
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(ii) Face-centred and end-centred unit cells.
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(i) Oxidation of a primary alcohol to carboxylic acid.
(ii) Oxidation of a primary alcohol to aldehyde.
(iii) Bromination of phenol to 2,4,6-tribromophenol.
(iv) Benzyl alcohol to benzoic acid.
(v) Dehydration of propan-2-ol to propene.
(vi) Butan-2-one to butan-2-ol.
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How the following conversions can be carried out?
(i) Propene to propan-1-ol
(ii) Ethanol to but-1-yne
(iii) 1-Bromopropane to 2-bromopropane
(iv) Toluene to benzyl alcohol
(v) Benzene to 4-bromonitrobenzene
(vi) Benzyl alcohol to 2-phenylethanoic acid
(vii) Ethanol to propanenitrile
(viii) Aniline to chlorobenzene
(ix) 2-Chlorobutane to 3, 4-dimethylhexane
(x) 2-Methyl-1-propene to 2-chloro-2-methylpropane
(xi) Ethyl chloride to propanoic acid
(xii) But-1-ene to n-butyliodide
(xiii) 2-Chloropropane to 1-propanol
(xiv) Isopropyl alcohol to iodoform
(xv) Chlorobenzene to p-nitrophenol
(xvi) 2-Bromopropane to 1-bromopropane
(xvii) Chloroethane to butane
(xviii) Benzene to diphenyl
(xix) tert-Butyl bromide to isobutyl bromide
(xx) Aniline to phenylisocyanide
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When low temperature favours the yield of ammonia why is it so high temperature of 700k is required in haber's process
If Low temperature is favourable then why are we keeping the temperature at 723K It should be like 273-278K
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