It becomes a nucleophile.So it can participhate in electrophilic reactions.
An ester bond will release an acid and an alcohol when hydrolyzed. This reaction is called ester hydrolysis and breaks the ester into its constituent carboxylic acid and alcohol through the addition of water.
You can convert a secondary alcohol to a primary alcohol by oxidizing the secondary alcohol using a strong oxidizing agent such as potassium permanganate (KMnO4) or chromium trioxide (CrO3) in acidic conditions. This reaction will cleave the carbon-carbon bond next to the hydroxyl group, forming a ketone intermediate, which can then be further oxidized to a primary alcohol.
A secondary alcohol undergoes oxidation to yield a ketone; a primary alcohol forms an aldehyde instead, and a tertiary alcohol usually does not form either a ketone or an alcohol, because the carbon having the OH group in a tertiary alcohol already has three bonds to other carbon atoms and therefore cannot form a double bond to oxygen without more extensive breaking of other bonds in the tertiary alcohol.
An alcohol, but it has cyclic rings and double bond.
It becomes a nucleophile.So it can participhate in electrophilic reactions.
An ester bond will release an acid and an alcohol when hydrolyzed. This reaction is called ester hydrolysis and breaks the ester into its constituent carboxylic acid and alcohol through the addition of water.
Tertiary alkyl halides are more reactive than primary alkyl halides because the carbon in a tertiary alkyl halide is more substitued and more stable due to hyperconjugation and steric hindrance. This makes the C-X bond weaker in tertiary alkyl halides, making them more reactive towards nucleophilic substitution reactions.
Ethylene (C2H4) is more reactive than ethane (C2H6) due to the presence of a pi bond in ethylene. The pi bond makes ethylene more susceptible to addition reactions with other molecules, while ethane lacks this double bond and is comparatively less reactive.
You can convert a secondary alcohol to a primary alcohol by oxidizing the secondary alcohol using a strong oxidizing agent such as potassium permanganate (KMnO4) or chromium trioxide (CrO3) in acidic conditions. This reaction will cleave the carbon-carbon bond next to the hydroxyl group, forming a ketone intermediate, which can then be further oxidized to a primary alcohol.
no
A secondary alcohol undergoes oxidation to yield a ketone; a primary alcohol forms an aldehyde instead, and a tertiary alcohol usually does not form either a ketone or an alcohol, because the carbon having the OH group in a tertiary alcohol already has three bonds to other carbon atoms and therefore cannot form a double bond to oxygen without more extensive breaking of other bonds in the tertiary alcohol.
Nitrogen Is Uncreative beacuase of the triple bond between 2 nitrogen atom,which have a bond enthalpy of 945kjmol-1,and this result for a fewer reactions of nitrogen.
Yes, a glycosidic bond between two monosaccharides can be classified as an ether bond because it involves the linking of two monosaccharides through the oxygen atom of one of the monosaccharides. It is not classified as an alcohol bond because an alcohol bond typically refers to a covalent bond between an -OH group and another atom in a molecule.
energy
Arsenic does not bond well with hydrogen, as arsenic hydrides are unstable and highly reactive compounds.
Metallic bond is the reaction between molecules within metals, called alkali reactive force.