In a primary (1°) alcohol, only attached to one alkyl group; In a secondary (2°) alcohol, attached two alkyl groups & tertiary (3°) alcohol, attached three alkyl groups
Actually, that person has you more confused. This is an easy way to remember what is 1 degree, 2 degree or 3 degree of Alcohols.
1 degree: R-- CH2 -- OH
2 degree: R2 -- CH -- OH
3 degree: R3 -- C -- OH
R = CH3
primary alcohol is more reactive than secondary alcohol when OH bond breaks while when CO bond breaks secondary alcohol is more reactive than primary alcohol because of the stability of carbocation due to more hyperconjunating structures(Pakistan)
This is true for dehydration of alcohols. The Tertiary alcohols have high stearic hindrance and after dehydration it is converted into an alkene so to reduce the stearic hindrance tertiary alcohols undergo fast dehydration process.
If the C atom bind to -OH only have 1 carbon chain it is a Primary Alcohol.Eg- CH3-CH2-OH If the C atom bind to -OH is binded to 2 carbon chains it is a secondry alcohol.Eg- OH l CH3-CH-CH3 If the C atom bind to -OH is binded to 3 carbon chains,it is a tritiary alcohol.Eg- OH l CH3-C-CH3 l CH3
All alcohols (except methanol) may undergo dehydration process in presence of dehydrating agent as sulphuric acid but their rates of reactions are different, tertiary alcohols dehydrate at normal temperature within seconds, secondary alcohols take 3 to 5 minutes and primary only on heating. (Lucas test).
A carbon atom directly attached to three other carbon atoms is a Tertiary carbon and alcohols in which 'OH' group is attached to tertiary carbon atom are tertiary alcohols as (CH3)3COH
lucas reagent
if it is a primary, secondary or tertiary alcohol
Tertiary react immediately, secondary takes about 5-10 minutes and primary alcohols do not react under standard conditions
A Tertiary alcohol
I'm guessing that because it is a tertiary alcohol, a lot of dehydration occurs. So you may need to distill repeatedly to get rid of the water?
you react the grignard with either an ester, an acid chloride or a ketone to get a tertiary alchohol. if you react a grignard reagent with an aldehyde you get a secondary alcohol and if you react the grignard with formaldehyde (methenal) you get a primary alchohol. same thing happens if u use R-Li instead of a grignard reagant.
it is a secondary alcohol
primary alcohol reacts the fastest towards oxidation followed by secondary alcohol and tertiary alcohol.
if it is a primary, secondary or tertiary alcohol
A secondary alcohol undergoes oxidation to yield a ketone; a primary alcohol forms an aldehyde instead, and a tertiary alcohol usually does not form either a ketone or an alcohol, because the carbon having the OH group in a tertiary alcohol already has three bonds to other carbon atoms and therefore cannot form a double bond to oxygen without more extensive breaking of other bonds in the tertiary alcohol.
Secondary and tertiary alcohols can form ketones. A primary alcohol will form an aldehyde.
Tertiary react immediately, secondary takes about 5-10 minutes and primary alcohols do not react under standard conditions
A Tertiary alcohol
Because 2- methylcyclohexanol is a secondary alcohol (2 R- groups) and can be oxidized to a ketone quite easity whereas 1- methylcyclohexanol is a tertiary alcohol (3 R- groups) and is not easily oxidized. Tertiary alcohols in general are very difficult to oxidize.
I'm guessing that because it is a tertiary alcohol, a lot of dehydration occurs. So you may need to distill repeatedly to get rid of the water?
you react the grignard with either an ester, an acid chloride or a ketone to get a tertiary alchohol. if you react a grignard reagent with an aldehyde you get a secondary alcohol and if you react the grignard with formaldehyde (methenal) you get a primary alchohol. same thing happens if u use R-Li instead of a grignard reagant.
Alkene, Tertiary amine(quinuclide bicyclic system), secondary alcohol, Quinoline(aromatic system, specifically 1-azanaphthalene) and Phenolic ethene.
A Secondary Alcohol When reduced with something like lithium aluminum hydride, a ketone results in a secondary alcohol.