Reactions of Alkynes : Addition due to excess HX yields a geminal dihaloalkane |
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date: 20-7-2019
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Date: 28-8-2018
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Date: 10-7-2019
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Date: 2-9-2018
2012
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Here, the electrophilic addition proceeds with the same steps used to achieve the product in Addition of a HX to an Internal Alkyne. The π electrons attacked the hydrogen, adding it to the carbon on the left (shown in blue). Why was hydrogen added to the carbon on left and the one on the right bonded to the Bromine?
Now, you will have your carbocation intermediate, which is followed by the attack of the Bromine to the carbon on the right resulting in a haloalkane product.
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