Identify the correct method for the synthesis of the compound shown below from the following alternatives.

Which one of the following methods are used to prepare Me₃COEt with good yield?

• Mixing EtONa with Me₂CCl

• Mixing Me₂CONa with EtCl

• Heating a mixture of (1:1) EtOH and Me₂COH in the presence of conc. H₂SO₄

• Treatment of Me₃COH with EtMgI

Under identical conditions, the SN₁ reaction will occur most efficiently with:

• tert-butyl chloride

• 1-chlorobutane

• 2-methyl-1-chloropropane

• 2-chlorobutane

Identify the method by which Me₃CCO₂H can be prepared:

• Treating 1 mole of MeCOMe with 2 moles of MeMgl

• Treating 1 mole of MeCO₃Me with 3 moles of MeMgI

• Treating 1 mole of MeCHO with 3 moles of MeMgl

• Treating 1 mole of dry ice with 1 mol of MeCMgI

The correct statement regarding the following compounds is

• all three compounds are chiral

• only I and II are chiral

• I and III are diastereomers

• only I and III are chiral

The ease of dehydrohalogenation of alkyl halide with alcoholic KOH is:

• 3° < 2° < 1°

• 3° > 2° > 1 °

• 3° < 2° > 1°

• 3° > 2° < 1 °

Boiling water reacts with C₆H₅N${}_2^{+}$Cl^- to give

• aniline

• benzylamine

• phenol

• benzaldehyde

When AgCl is treated with KCN

• Ag is precipitated

• a complex ion is formed

• double decomposition takes place

• no reaction takes place

Which one of the following compounds is most reactive towards nucleophilic addition?

• CH₃CHO

• PhCOCH₃

• PhCOPh

• CH₃COCH₃

Which reaction is used for the preparation of acetophenone ?

• Reimer-Tiemann reaction

• Wurtz-Fittig reaction

• Friedel-Craft's reaction

• Cannizaro's reaction