322893 Which of the following pairs of the compounds can be used as starting materials in the synthesis of 2-phenyl-2-pentanol?

322895 Propene when treated with cold conc. ${\mathrm{H}}_2{\mathrm{SO}}_4$ forms a compound which on heating with water gives

322896 Which one/ones of the following reactions will yield 2-propanol?
I. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\text{ + }{\text{H}}_{\text{2}}\text{O}\stackrel{{\text{H}}^{\text{ + }}}{\to }$
II. $\text{C}{\text{H}}_{\text{3}}\text{ - CHO}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) C}{\text{H}}_{\text{3}}\text{MgI}}{\to }}$
III.$\text{C}{\text{H}}_{\text{2}}\text{O}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) }{\text{C}}_{\text{2}}{\text{H}}_{\text{5}}\text{MgI}}{\to }}$
IV. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\stackrel{\text{ Neutral KMn}{\text{O}}_{\text{4}}}{\to }$

322897

‘X’ would be

322893 Which of the following pairs of the compounds can be used as starting materials in the synthesis of 2-phenyl-2-pentanol?

322894 The acid catalysed hydration of alkene involves the following three steps.
I. Nucleophilic attack of water on carbocation.
II. Protonation of alkene to form carbocation by the electrophilic attack of ${\mathrm{H}}_3{\mathrm{O}}^{+}$.
III. Deprotonation to form an alcohol.
Identify the sequence for the mechanism of reation in the acid catalysed hydration of alkenes.

322895 Propene when treated with cold conc. ${\mathrm{H}}_2{\mathrm{SO}}_4$ forms a compound which on heating with water gives

322896 Which one/ones of the following reactions will yield 2-propanol?
I. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\text{ + }{\text{H}}_{\text{2}}\text{O}\stackrel{{\text{H}}^{\text{ + }}}{\to }$
II. $\text{C}{\text{H}}_{\text{3}}\text{ - CHO}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) C}{\text{H}}_{\text{3}}\text{MgI}}{\to }}$
III.$\text{C}{\text{H}}_{\text{2}}\text{O}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) }{\text{C}}_{\text{2}}{\text{H}}_{\text{5}}\text{MgI}}{\to }}$
IV. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\stackrel{\text{ Neutral KMn}{\text{O}}_{\text{4}}}{\to }$

322897

‘X’ would be

322893 Which of the following pairs of the compounds can be used as starting materials in the synthesis of 2-phenyl-2-pentanol?

322894 The acid catalysed hydration of alkene involves the following three steps.
I. Nucleophilic attack of water on carbocation.
II. Protonation of alkene to form carbocation by the electrophilic attack of ${\mathrm{H}}_3{\mathrm{O}}^{+}$.
III. Deprotonation to form an alcohol.
Identify the sequence for the mechanism of reation in the acid catalysed hydration of alkenes.

322895 Propene when treated with cold conc. ${\mathrm{H}}_2{\mathrm{SO}}_4$ forms a compound which on heating with water gives

322896 Which one/ones of the following reactions will yield 2-propanol?
I. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\text{ + }{\text{H}}_{\text{2}}\text{O}\stackrel{{\text{H}}^{\text{ + }}}{\to }$
II. $\text{C}{\text{H}}_{\text{3}}\text{ - CHO}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) C}{\text{H}}_{\text{3}}\text{MgI}}{\to }}$
III.$\text{C}{\text{H}}_{\text{2}}\text{O}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) }{\text{C}}_{\text{2}}{\text{H}}_{\text{5}}\text{MgI}}{\to }}$
IV. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\stackrel{\text{ Neutral KMn}{\text{O}}_{\text{4}}}{\to }$

322897

‘X’ would be

322893 Which of the following pairs of the compounds can be used as starting materials in the synthesis of 2-phenyl-2-pentanol?

322894 The acid catalysed hydration of alkene involves the following three steps.
I. Nucleophilic attack of water on carbocation.
II. Protonation of alkene to form carbocation by the electrophilic attack of ${\mathrm{H}}_3{\mathrm{O}}^{+}$.
III. Deprotonation to form an alcohol.
Identify the sequence for the mechanism of reation in the acid catalysed hydration of alkenes.

322895 Propene when treated with cold conc. ${\mathrm{H}}_2{\mathrm{SO}}_4$ forms a compound which on heating with water gives

322896 Which one/ones of the following reactions will yield 2-propanol?
I. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\text{ + }{\text{H}}_{\text{2}}\text{O}\stackrel{{\text{H}}^{\text{ + }}}{\to }$
II. $\text{C}{\text{H}}_{\text{3}}\text{ - CHO}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) C}{\text{H}}_{\text{3}}\text{MgI}}{\to }}$
III.$\text{C}{\text{H}}_{\text{2}}\text{O}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) }{\text{C}}_{\text{2}}{\text{H}}_{\text{5}}\text{MgI}}{\to }}$
IV. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\stackrel{\text{ Neutral KMn}{\text{O}}_{\text{4}}}{\to }$

322897

‘X’ would be

322893 Which of the following pairs of the compounds can be used as starting materials in the synthesis of 2-phenyl-2-pentanol?

322894 The acid catalysed hydration of alkene involves the following three steps.
I. Nucleophilic attack of water on carbocation.
II. Protonation of alkene to form carbocation by the electrophilic attack of ${\mathrm{H}}_3{\mathrm{O}}^{+}$.
III. Deprotonation to form an alcohol.
Identify the sequence for the mechanism of reation in the acid catalysed hydration of alkenes.

322895 Propene when treated with cold conc. ${\mathrm{H}}_2{\mathrm{SO}}_4$ forms a compound which on heating with water gives

322896 Which one/ones of the following reactions will yield 2-propanol?
I. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\text{ + }{\text{H}}_{\text{2}}\text{O}\stackrel{{\text{H}}^{\text{ + }}}{\to }$
II. $\text{C}{\text{H}}_{\text{3}}\text{ - CHO}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) C}{\text{H}}_{\text{3}}\text{MgI}}{\to }}$
III.$\text{C}{\text{H}}_{\text{2}}\text{O}\underset{\text{ (ii) }{\text{H}}_{\text{2}}\text{O}}{\overset{\text{ (i) }{\text{C}}_{\text{2}}{\text{H}}_{\text{5}}\text{MgI}}{\to }}$
IV. $\text{C}{\text{H}}_{\text{2}}\text{ = CH - C}{\text{H}}_{\text{3}}\stackrel{\text{ Neutral KMn}{\text{O}}_{\text{4}}}{\to }$

322897

‘X’ would be