it goes from a high point to a low point back to a high point or vice versa.
Is not adequate to prevent dehydration effects in the cell
Answer:
See explanation below
Explanation:
In this case, we need to see which is the structure of this compound. Now, racemization occurs basically because we are in an aqueous basic medium, and the ketone can reacts again with water in the medium to form the starting reagent.
First, the base will take out the Alpha hydrogen from the ketone, then, the negative charge goes down and opens up the carbonile group, forming a double bond in there. Later, with the water of the medium, it reacts and substract a proton, and then, with keto enolic equilibrium, forms again the ketone, but this ketone is different from the start, it will be the R isomer which is not optically active.
See picture below for mechanism
Answer:
3)The rate of the forward reaction is equal to the rate of the reverse reaction
It's only a small difference (103 degrees versus 104 degrees in water),
and I believe the usual rationalization is that since F is more
electronegative than H, the electrons in the O-F bond spend more time
away from the O (and close to the F) than the electrons in the O-H bond.
That shifts the effective center of the repulsive force between the
bonding pairs away from the O, and hence away from each other. So the
repulsion between the bonding pairs is slightly less, while the
repulsion between the lone pairs on the O is the same -- the result is
the angle between the bonds is a little less.
Hope this helps!