2-propanol is a primary alcohol and 1-propanol is a primary alcohol. We can convert secondary alcohol to primary alcohol in several steps. 2-propanol and 1-propanol are isomers of each other.
1-propanol is also known as propan-1-ol, 1-propyl alcohol, n-propyl alcohol, and n-propanol.
2-Propanol can be dehydrated by dehydrators such as concentrated sulfuric acid or alumina or diphosphorous pentoxide. When propanol is heated with one of these dehydrator, propene (an alkene) is given as the product.
When propene reacts with HBr in the presence of organic peroxide, HBr molecule is added across the double bond according to the anti-Markovnikov rule. As the product, 1-bromopropane (an alkyl halide) is given.
With dilute NaOH, bromine atom is replaced by hydroxyl group of NaOH and 1-propanol is given as the product.
Written by: Heshan Nipuna
Published date: 2019-12-13
Last modified: 2013-12-13
Questions asked by students
You know primary alcohols and secondory alcohols answer in different way to Lucas' reagent (anhydrous ZnCl2 / concentrated HCl).
With Lucas' reagent, 2-propanol (secondary alcohol) gives a turbidity around five minutes. But, 1-propanol (primary alcohol) does not a turbity with Lucas' reagent. So, according tothe time this turditity is given, 1-propanol and 2-propanol can be identified.
You cannot prepare 1-propanol from alkene hydration reaction because propene hydration gives 1-propanol again.
No, you cannot always prepare primary alcohol from this way of reactions. In this method, a bromine atom is connected to the a carbon atom which is located at the end of the chain. If this possibility is there in that secondary alcohol, a primary alcohol can be prepared.
Around carbinol carbon atom, there are two methyl groups. Therefore 2-propanol is a secondary alcohol.
Propan-2-ol and 2-propanol both are same compound and those two names are two different ways to write IUPAC name for that compound.
To prepare propene by propan-2-ol, concentrated H2SO4 acid is heated with propan-2-ol .
You have to put a dash sign after a number in the IUPAC nomenclature. So correct names should be, 2-propanol to 1-propanol.
Both propan-2-ol and propan-1-ol give propene with dehydrators.
You can dehydrate propyl alcohol to prepare propene.