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hey guys, professor Dave here. I'd like to talk to you a little bit about elimination reactions, specifically the E2 reaction. so in any elimination reaction two groups from adjacent carbons are removed and replaced by a double bond between those two carbons so let's take a look here's just a a bromopropane and so here is hydrogen and here's the bromine, these are the two adjacent carbons so what's going on is some nucleophile, let's say hydroxide in this case instead of doing a substitution reaction we're going to do an acid-base reaction, that means that a proton will be extracted ts notice that the arrow goes from the hydroxide directly to this proton and then the electrons in the carbon-hydrogen bond are going to go and form the double bond between these two carbons and then just as with a substitution reaction a leaving group must leave so this is what's left, propene and then we have water and the bromide ion and so

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