1) Alcohols can be prepared from alkenes through acid-catalyzed hydration, where water is added across the carbon-carbon double bond.
2) The addition of water follows Markovnikov's rule, forming the carbocation next to the most substituted carbon.
3) Hydration of alkenes produces primary alcohols without rearrangement or formation of carbocations.
1) Alcohols can be prepared from alkenes through acid-catalyzed hydration, where water is added across the carbon-carbon double bond.
2) The addition of water follows Markovnikov's rule, forming the carbocation next to the most substituted carbon.
3) Hydration of alkenes produces primary alcohols without rearrangement or formation of carbocations.
1) Alcohols can be prepared from alkenes through acid-catalyzed hydration, where water is added across the carbon-carbon double bond.
2) The addition of water follows Markovnikov's rule, forming the carbocation next to the most substituted carbon.
3) Hydration of alkenes produces primary alcohols without rearrangement or formation of carbocations.
1) Alcohols can be prepared from alkenes through acid-catalyzed hydration, where water is added across the carbon-carbon double bond.
2) The addition of water follows Markovnikov's rule, forming the carbocation next to the most substituted carbon.
3) Hydration of alkenes produces primary alcohols without rearrangement or formation of carbocations.
OH vinylic alcohol x Electrophilic Addition CHI = CH -
Rate of a stability of x alcohol CH2CH-cHy-oH allylic =
Run Carbocation Benzylic alcohol CHOH Mercuration) 2) OMDM (Ony Mercuration De
CH2-OH CH2-OH ) HgCOAC2
OH tRO dre-or R
cte R-CH CH2 2) CH - - =
OH NaBHn CH2 =
ethylene glycol dia-or Source ofOH: -
H20 glycerol Source of H: -NaBHy
PreparationofAlcohols NOTE: addition From Alkenes Addition ofWater x Ants ) Markovnikoy'srule a) Acidcatalysed hydration > No rearrangement Reagent: bil. H2SO4 or HT H20 or Hot > No carbocation
