CH3 H3C OH Br2 H20 CH3 CH3 H3C H3C Br Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called i halohydrin. Halohydrin formation, however, does not result from the addition of HO-Br, for example. Instead the addition is done inc rectly by reaction of the alkene with Br2 in the presence of water. The reaction also works with Cl, to give chlorohydrins instead of romohydrins. The reaction proceeds through a cyclic intermediate known as a bromonium ion. In the second step of the reaction, water is the nucleophile and reacts with the bromonium ion to yield the product. The reaction can also proceed using an alcohol as the solvent instead of water, to give a 1,2-haloether. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions H. | CH3 но CH3 HỘ CH3 HO CH3 H3C H3C Açtivate Windows Go to Settings to activate W Br Br

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Chapter1: Chemical Foundations
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Draw curved arrows to show the movement of electrons in this step of the mechanism. 

CH3
H3C OH
Br2
H20
CH3
CH3
H3C
H3C
Br
Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called i halohydrin. Halohydrin formation, however, does
not result from the addition of HO-Br, for example. Instead the addition is done inc rectly by reaction of the alkene with Br, in the
presence of water. The reaction also works with Cl, to give chlorohydrins instead of romohydrins.
The reaction proceeds through a cyclic intermediate known as a bromonium ion In th e second step of the reaction, water is the
nucleophile and reacts with the bromonium ion to yield the product.
The reaction can also proceed using an alcohol as the solvent instead of water, to give a 1,2-haloether.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
H.
| CH3
HOt
CH3
HỘ
CH3 H3Q
CH3
H3C
H3C
Activate Windows
Go to Settings to actuate W
Br
Br
Transcribed Image Text:CH3 H3C OH Br2 H20 CH3 CH3 H3C H3C Br Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called i halohydrin. Halohydrin formation, however, does not result from the addition of HO-Br, for example. Instead the addition is done inc rectly by reaction of the alkene with Br, in the presence of water. The reaction also works with Cl, to give chlorohydrins instead of romohydrins. The reaction proceeds through a cyclic intermediate known as a bromonium ion In th e second step of the reaction, water is the nucleophile and reacts with the bromonium ion to yield the product. The reaction can also proceed using an alcohol as the solvent instead of water, to give a 1,2-haloether. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions H. | CH3 HOt CH3 HỘ CH3 H3Q CH3 H3C H3C Activate Windows Go to Settings to actuate W Br Br
CH3
H3C OH
CH3
Br2
CH3
H3C
H20
Br
Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called a halohydrin. Halohydrin formation, however, does
not result from the addition of HO-Br, for example. Instead the addition is done indirectly by reaction of the alkene with Br, in the
presence of water. The reaction also works with Cl, to give chlorohydrins instead of bromohydrins.
The reaction proceeds through a cyclic intermediate known as a bromonium ion. In the second step of the reaction, water is the
nucleophile and reacts with the bromonium ion to yield the product.
The reaction can also proceed using an alcohol as the solvent instead of water, to give a 1,2-haloether.
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
CH3
CH3
H2Q
CH3
CH3
H3C
H3C
:Br
:Br:
Activate Windows
Go to Settingsto activate W
Transcribed Image Text:CH3 H3C OH CH3 Br2 CH3 H3C H20 Br Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called a halohydrin. Halohydrin formation, however, does not result from the addition of HO-Br, for example. Instead the addition is done indirectly by reaction of the alkene with Br, in the presence of water. The reaction also works with Cl, to give chlorohydrins instead of bromohydrins. The reaction proceeds through a cyclic intermediate known as a bromonium ion. In the second step of the reaction, water is the nucleophile and reacts with the bromonium ion to yield the product. The reaction can also proceed using an alcohol as the solvent instead of water, to give a 1,2-haloether. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CH3 CH3 H2Q CH3 CH3 H3C H3C :Br :Br: Activate Windows Go to Settingsto activate W
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