The molecular formula for 2-methyl-1-propanol is C4H10O.
Propanol and isopropanol are isomers. Isopropanol is the structural isomer of propanol. It has a strong smell and is without any color.
Yes, 1-chloro-2-propanol is chiral because it has a chiral center at the carbon atom bonded to the chlorine atom and two methyl groups.
When 2-propanol reacts with NaOCl, the main organic compound formed is chloropropanol. This compound can be either 1-chloropropanol or 2-chloropropanol, depending on the position of the chlorine atom relative to the hydroxyl group in the 2-propanol molecule.
a primary alcohol
The systematic name for propanol is 1-propanol. It is also known as n-propanol.
When propanol (1-propanol) is heated, it can undergo combustion to produce carbon dioxide, water, and heat. It can also undergo dehydration to form propene (an alkene) and water. Additionally, under certain conditions, propanol can isomerize to form other isomers such as 2-propanol (isopropanol).
Yes, 2-methyl-1-propanol is considered polar due to the presence of an alcohol group (OH) which creates a dipole moment, making it soluble in polar solvents.
Yes, 2,3-epoxy-1-propanol is soluble in water. Its chemical structure contains a hydroxyl group (-OH) that can form hydrogen bonds with water molecules, making it soluble.
To convert 2-propanol into pseudonitrol, you need to react it with a mixture of nitric acid and sulfuric acid at elevated temperatures. This process will lead to the formation of pseudonitrol, which is a nitro compound derived from the alcohol.
The six constitutional isomers of C3H6O are: acetone, propanal, isopropanol, methoxyethane, propanone, and oxetane.
The standard enthalpy of combustion for 1-propanol is approximately -2026 kJ/mol, meaning that the heat released when 1 mol of 1-propanol is completely burned is 2026 kJ.