2-Methyl-1-propanol is a primary alcohol and so will not react with Lucas reagent at room temperature.
Cyclopentanol is a secondary alcohol and so will react with Lucas reagent in 3-5 minutes (solution turns cloudy). Cyclopentyl chloride is the result.
1-Methylcyclopentanol is a tertiary alcohol and so will react immediately with Lucas reagent to produce turbidity. 1-Chloro-1-methylcyclopentanol is the result.
there is no reaction you bitcheees
acetone
The amount of product formed will be limited reagent in a reaction
Lucas reagent is used to test for the presence of alcohols in a substance. It is made from anhydrous zinc chloride and concentrated hydrochloric acid.
The limiting reagent is entirely used at the end of a chemical reaction.
The Lucas test is applicable for cyclohexanol. Cyclohexanol is a secondary alcohol and s reported to react with the Lucas reagent after a few minutes.
balanced equation for ethanol and lucas reagent
methylhexanoic
Since 2-butanol is a secondary alcohol, it will form a cloudy precipitate after approximately 5-6 minutes.
ethyl magnesium bromide to propanol
It will be a ketone attached to the second carbon of the propanol (in place of the OH) if treated with a mild oxidant.
acetone
In a chemical reaction the limiting reagent is the compound totally consumed when the reaction is complete.
what is the reaction mechanism between wagner's reagent and alkaloids
The amount of product formed will be limited reagent in a reaction
Lucas reagent is used to test for the presence of alcohols in a substance. It is made from anhydrous zinc chloride and concentrated hydrochloric acid.
The limiting reagent is entirely used at the end of a chemical reaction.
No, its reaction with SO2(aq) gives schiff's reagent.