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It's not the healthiest thing you could put in your bloodstream, but if you haven't been exposed for large doses over a long period of time, you should be fine. Just filter your MCat through some cleanexes next time ;P.

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14y ago

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How is benzaldehyde different from formaldehyde?

Benzaldehyde has a benzene ring where formaldehyde has a hydrogen atom. (C6H5CHO as opposed to HCHO). Formaldehyde is used as a biocide and a disinfectant. It is a nasty substance and may be a carcinogen. Benzaldehyde on the other hand is used as a food additive to give an almond flavour.


How many grams are in 5 ml of 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.


What is density of benzaldehyde?

The density of benzaldehyde is 1,044 g/cm3.


How do you spell benzaldehyde?

That is the correct spelling of "benzaldehyde" (aromatic compound found in almonds).


What is the smell of benzaldehyde like?

The smell of benzaldehyde is often described as being similar to almonds or cherries.


Is benzaldehyde soluble in sodium hydroxide?

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.


Is benzaldehyde miscible immiscible or partially miscible?

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.


What is the density of benzaldehyde?

The density of benzaldehyde is approximately 1.041 g/cm3 at 20°C.


What is the major product of auto oxidation of benzaldehyde?

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.


Schiff base of aniline and benzaldehyde?

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.


How do you convert benzaldehyde to benzoyl chloride?

Benzaldehyde can be converted to benzoyl chloride by reacting with thionyl chloride (SOCl2) under reflux conditions. The reaction involves replacement of the aldehyde group with a chlorine atom to form the benzoyl chloride. Attention must be paid as thionyl chloride is a corrosive and toxic compound, so the reaction should be performed in a fume hood and with appropriate safety precautions.


What is benzaldehyde?

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.