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Topic: synthesis  (Read 3409 times)

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Offline fishyfisherman77

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synthesis
« on: November 21, 2009, 07:57:42 AM »
In this problem-                        Br
                                                        |
H3C-C=CH     +   2 HBr   --->      H3C-C-CH3
                                                        |
                                                       Br

The triple bond goes away why?

& This problem-                 

                                           Br
                                           |
H3C-C=CH      +  HBr ---> H3C-C=CH2
         






why/how does the triple bond go to double bond?




( THE RED BONDS ARE TRIPLE BONDS )

Offline DrCMS

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Re: synthesis
« Reply #1 on: November 21, 2009, 08:14:14 AM »
because it reacts with the HBr.

Offline fishyfisherman77

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Re: synthesis
« Reply #2 on: November 21, 2009, 08:25:46 AM »
so with 2 halogens it always goes from triple to single


and hydrogen and halogen it always goes triple to double?
im so cofnsuded

Offline sjb

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Re: synthesis
« Reply #3 on: November 21, 2009, 08:32:07 AM »
so with 2 halogens it always goes from triple to single


and hydrogen and halogen it always goes triple to double?
im so cofnsuded

Not necessarily. With two equivalents of Br2 you'd get triple to single, just as with one equivalent of HBr you'd go from triple to double, or double to single.

Offline fishyfisherman77

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Re: synthesis
« Reply #4 on: November 21, 2009, 09:33:31 AM »
thanks people like  u make this stuff easy :o)

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