In the Fischer esterification reaction, a carboxylic acid reacts with an excess of alcohol in acidic conditions to form an ester
. During the reaction the sp2sp2 hybridized carbonyl carbon of the acid forms an sp3sp3 hybridized intermediate before returning to sp2sp2 hybridization in the product. Draw the structure of the neutral sp3sp3 hybridized intermediate and the ester product in the reaction between pentanoic acid and n‑propanol.
Esterification is a reaction of an alkanol and an alkanoic acid to yield an ester and water as products. It is analogous to inorganic neutralization reaction.
The process may be acid catalyzed. As mentioned in the question, the process of ester formation between pentanoic acid and n‑propanol first involves the carbonyl in going through an sp3 hybridized intermediate before returning to sp2 hybridized state in the product.
The image of the neutral form of this intermediate as well as the final structure of the ester are both shown in the image attached to this answer.
Explanation:When aqueous hydroiodic acid and aqueous potassium sulfite are mixed the products obtained are potassium iodide and sulfurous acid.Both reactants are ionic compounds and they undergo double replacement reaction.In a double replacement reaction the parts of the ionic compounds are changed.The product is obtained by combinig cation of one compound with anion of other compound.so in above reaction sulfurous acid is obtained which is in gaseous form and potassium iodide is an ionic compound.
