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Write the name of the reagent and the equation for the preparation of the following ether by Williamson’s synthesis:
1-Propoxypropane
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Write the name of the reagent and the equation for the preparation of the following ether by Williamson’s synthesis:
Ethoxybenzene
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Write the name of the reagent and the equation for the preparation of the following ether by Williamson’s synthesis:
2-Methoxy-2-methylpropane
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Write the name of the reagent and equation for the preparation of the following ethers by Williamson’s synthesis:
1-Methoxyethane
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Illustrate with examples the limitations of Williamson synthesis for the preparation of certain types of ethers.
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How is 1-propoxypropane synthesised from propan-1-ol? Write mechanism of this reaction.
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Preparation of ethers by acid dehydration of secondary or tertiary alcohols is not a suitable method. Give reason.
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Explain the following with an example.
Williamson ether synthesis
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How will you bring about the following conversion?
Benzene to biphenyl
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How the following conversion can be carried out?
Benzene to diphenyl
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Explain effects of lanthanoid contraction.
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What are the consequences of lanthanoid contraction?
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Draw labelled diagram Dialysis.
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Name an important alloy which contains some of the lanthanoid metals.
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Name an important alloy which contains some of the lanthanoid metals. Mention its uses.
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8 g of glucose, C6H12O6 (Molar Mass = 180 g mol−1) is dissolved in 1 kg of water in a sauce pan. At what temperature will this solution boil?
(Kb for water = 0.52 K kg mol−1, boiling point of pure water = 373.15 K)
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Calculate the boiling point of solution when 4g of MgSO4 (M= 120 g mol-1) was dissolved in 100g of water, assuming MgSO4 undergoes complete ionization. (Kb for water = 0.52 K kgmol-1)
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Write the structures of A and B in the following reactions

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Predict the products of the following reactions:

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Illustrate the following reaction giving suitable example in each case: Diazotisation
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