by grignard reaction.....
Acetone can be converted to t-butyl alcohol using a Grignard reaction. First, react acetone with magnesium metal to form a Grignard reagent. Then, the Grignard reagent reacts with isobutylene (2-methylpropene) to yield t-butyl alcohol. This process involves multiple steps and careful control of reaction conditions to ensure a successful conversion.
T-butyl chloride is insoluble in water because it is a nonpolar molecule, which does not interact favorably with the polar water molecules. T-butyl alcohol, on the other hand, is soluble in water due to the presence of the hydroxyl group, which can form hydrogen bonds with water molecules, enhancing its solubility.
t-Butyl alcohol is soluble in water due to its hydroxyl group, in alcohol solvents due to its similar structure, and in cyclohexane due to its nonpolar nature.
When t-butyl alcohol (C4H10O) reacts with HCl, an acid-catalyzed dehydration reaction takes place to form t-butyl chloride (C4H9Cl) as the main product. The reaction involves the removal of a water molecule from t-butyl alcohol in the presence of HCl. The formula for the reaction is C4H10O + HCl -> C4H9Cl + H2O.
The IUPAC name for t-butyl is 2-methylpropane.
Acetone can be converted to t-butyl alcohol using a Grignard reaction. First, react acetone with magnesium metal to form a Grignard reagent. Then, the Grignard reagent reacts with isobutylene (2-methylpropene) to yield t-butyl alcohol. This process involves multiple steps and careful control of reaction conditions to ensure a successful conversion.
you would get t-butyl chloride
T-butyl chloride is insoluble in water because it is a nonpolar molecule, which does not interact favorably with the polar water molecules. T-butyl alcohol, on the other hand, is soluble in water due to the presence of the hydroxyl group, which can form hydrogen bonds with water molecules, enhancing its solubility.
Methanol is the most volatile compound among the options listed. It has the lowest boiling point and highest vapor pressure compared to acetone, 2-butanone, and t-butyl chloride.
A water molecule is removed when alcohols are dehydrated. Then a alkyne is formed. When t-butyl alcohol dehydrated,2-butyne is formed.
t-Butyl alcohol is soluble in water due to its hydroxyl group, in alcohol solvents due to its similar structure, and in cyclohexane due to its nonpolar nature.
Acetone 0.79; t-Butyl alcohol 0.79; Isopropyl alcohol 0.79; Methyl alcohol 0.79; Propionaldehyde 0.81
When t-butyl alcohol (C4H10O) reacts with HCl, an acid-catalyzed dehydration reaction takes place to form t-butyl chloride (C4H9Cl) as the main product. The reaction involves the removal of a water molecule from t-butyl alcohol in the presence of HCl. The formula for the reaction is C4H10O + HCl -> C4H9Cl + H2O.
The pH of t-butyl alcohol (tert-butyl alcohol or t-BuOH) is not straightforward to define because it is a neutral organic compound that does not dissociate in water to produce hydrogen ions (H⁺). Instead, it acts as a non-volatile solvent and has a weakly acidic nature. When dissolved in water, it typically has a pH around 7, but this can vary slightly depending on concentration and temperature.
addition of potassium dichromate will create a colour change from orange to a blue/green colour in isopropanol, and will not change in t-butyl (assuming t-butyl is 2-methylpropan-2-ol)If the OH group on the t-butyl is on one of the ends (2-methyl propan-1-ol), you would then add tollens reagent, and the isopropanol (now oxidised to propanal) would form a silver mirror on the sides of the test/boiling tube you are reacting in.
The IUPAC name for t-butyl is 2-methylpropane.
T-butyl refers to the tert-butyl group, which consists of three methyl groups attached to a central carbon atom. N-butyl, on the other hand, refers to the normal butyl group, which consists of a four-carbon chain with a linear structure. T-butyl is more bulky and branched compared to n-butyl, which affects its reactivity and steric hindrance in chemical reactions.