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.
a reaction happens
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.
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.
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
When a bond between two atoms breaks, energy is either absorbed or released depending on the specific bond. If the bond is broken by adding energy, such as heat or light, it is an endothermic process. If the bond is broken by releasing energy, it is an exothermic process.
Chemical duhhh
Homolytic bond dissociation energy is when a covalent bond breaks evenly, with each atom keeping one electron. Heterolytic bond dissociation energy is when a covalent bond breaks unevenly, with one atom keeping both electrons.
Shared experiences and common goals are two of the primary reasons for a strong team bond.
An alcohol, but it has cyclic rings and double bond.
it rises