Benzaldehyde has a structural formula of C6H5CHO and a Hill formula of C7H6O. It is a liquid at STP and has a molar mass of 106.122 grams per mole.
Benzaldehyde's liquid density is 1.0415 g/mL. This means 5 mL of benzaldehyde is equivalent to 5.2075 g of liquid benzaldehyde.
The smell of benzaldehyde is often described as being similar to almonds or cherries.
Yes, benzaldehyde is soluble in sodium hydroxide to some extent due to the formation of a water-soluble sodium salt of benzaldehyde through a process known as neutralization. The solubility of benzaldehyde in sodium hydroxide will depend on various factors such as temperature and concentration.
Benzaldehyde is partially miscible in water, meaning that it can mix with water to some extent but not completely. This is due to the polarity of benzaldehyde, which allows for some interaction with water molecules.
The density of benzaldehyde is approximately 1.041 g/cm3 at 20°C.
benzaldehyde
Benzaldehyde's liquid density is 1.0415 g/mL. This means 5 mL of benzaldehyde is equivalent to 5.2075 g of liquid benzaldehyde.
The density of benzaldehyde is 1,044 g/cm3.
Benzylidenecyclopentanone Draw its structure by attaching C6H5-CH= to carbon 2 of cyclopentanone.
That is the correct spelling of "benzaldehyde" (aromatic compound found in almonds).
The smell of benzaldehyde is often described as being similar to almonds or cherries.
Yes, benzaldehyde is soluble in sodium hydroxide to some extent due to the formation of a water-soluble sodium salt of benzaldehyde through a process known as neutralization. The solubility of benzaldehyde in sodium hydroxide will depend on various factors such as temperature and concentration.
Benzaldehyde is partially miscible in water, meaning that it can mix with water to some extent but not completely. This is due to the polarity of benzaldehyde, which allows for some interaction with water molecules.
The density of benzaldehyde is approximately 1.041 g/cm3 at 20°C.
The major product of the autooxidation of benzaldehyde is a crystalline white precipitate of benzoic acid. When few drops of benzaldehyde is exposed to the atmosphere by using a watchglass, it is oxidized to form carboxylic acid salt.
The Schiff base formed from aniline and benzaldehyde is N-phenylideneaniline. This compound is a imine derivative and is commonly used in organic synthesis reactions. It is formed by the condensation of aniline and benzaldehyde in the presence of a suitable catalyst.
Benzaldehyde is a compound with the chemical formula C7H6O and a distinct almond-like scent. It is commonly used in the production of dyes, perfumes, and flavorings. Benzaldehyde can also be found naturally in certain fruits and nuts.