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The answer here is 4. I was ruling for 2. It's for sure not 1,3 or 5. Anyone can explain?
yo...
Since it's Sn2, we know it's not gonna give a racemic mixture; rather, it will give an inversion. In this case from S to R. Sn2 reaction rate does depend on the concentration of the nucleophile, so second choice is out too. Carbocations are formed in Sn1 reactions; in Sn2 you get a transition state with partial charges - third answer is out. Choice 4 is the correct one since Sn2 does give an inverted product.
Another easy way to tackle problems of this sort is by looking at the choices. The last two choices are opposites of each other, so guess which 2 choices you have to choose from.🙄
In short, the correct answer is 4.
Cheers
why guess when you can just look at the rxn and see it uses ACETONE as the solvent....since ACETONE is a polar aprotic solvent you know its SN2...and from there choose the SN2 answer stating that SN2 does a "backside" concerted attack on the carbon which causes and inversion....that question should take no more than 10 seconds.
I think his point was that this is a very simple question compared to others that may be asked on the test (it really is...). If it takes someone a while to get this, it might take them a really long time to get some of the harder questions.
This was textbook SN2 = inversion.