322880 The acid-catalyzed hydration of alkenes 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 reaction in the acid-catalyzed hydration of alkenes.

322881 The reagent required to convert propene to 1 propanol is

322882
cannot be prepared by

322883 The reaction of Grignard reagent with formaldehyde followed by acidification gives

322884

B and C are, respectively,

322880 The acid-catalyzed hydration of alkenes 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 reaction in the acid-catalyzed hydration of alkenes.

322881 The reagent required to convert propene to 1 propanol is

322882
cannot be prepared by

322883 The reaction of Grignard reagent with formaldehyde followed by acidification gives

322884

B and C are, respectively,

322880 The acid-catalyzed hydration of alkenes 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 reaction in the acid-catalyzed hydration of alkenes.

322881 The reagent required to convert propene to 1 propanol is

322882
cannot be prepared by

322883 The reaction of Grignard reagent with formaldehyde followed by acidification gives

322884

B and C are, respectively,

322880 The acid-catalyzed hydration of alkenes 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 reaction in the acid-catalyzed hydration of alkenes.

322881 The reagent required to convert propene to 1 propanol is

322882
cannot be prepared by

322883 The reaction of Grignard reagent with formaldehyde followed by acidification gives

322884

B and C are, respectively,

322880 The acid-catalyzed hydration of alkenes 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 reaction in the acid-catalyzed hydration of alkenes.

322881 The reagent required to convert propene to 1 propanol is

322882
cannot be prepared by

322883 The reaction of Grignard reagent with formaldehyde followed by acidification gives

322884

B and C are, respectively,