Chemistry, 06.11.2019 23:31, michell282
Aldehydes and ketones can be halogenated at their α-position by reaction with cl2, br2, or i2, under acidic conditions. using br2 under acidic conditions, an intermediate enol is formed which adds bromine at the α-position. the reaction stops after the addition of one bromine because the electron-withdrawing halogen decreases the basicity of the carbonyl oxygen, making the protonation less favorable. draw curved arrows to show the movement of electrons in this step of the mechanism.
Answers: 1
Chemistry, 22.06.2019 23:00, tovarclaudia055
What does a numerical subscript following an element in a chemical formula mean?
Answers: 1
Aldehydes and ketones can be halogenated at their α-position by reaction with cl2, br2, or i2, under...
Mathematics, 14.09.2019 05:30
Mathematics, 14.09.2019 05:30
Mathematics, 14.09.2019 05:30
Mathematics, 14.09.2019 05:30
Mathematics, 14.09.2019 05:30