what is the better nucleophile and why?
which is a better nucleophile Br or OH why?
plus state the reason why the following nucleophile is better nucleophile from the reasons given in pic. Question 2 16 pts H2S vs. H2O A Pair 1 B VS. в OH Pair 2 VS. CI (protic solvent) OH A vs. H2O Pair 3 B Pair 4 " CH,CH NH2 vs. CH.CH OH Pair 5 B (aprotic solvent) A Pair 6 B NH2 o vs. Pair 7 F vs. M Pair 8 B A B For each of the given pairs...
Circle the better nucleophile Circle the better nucleophile . . _0 . 0 ܐ . ܂ VS As Hac _°NH
5) Iodine is a better leaving group than bromine. But iodine is a better nucleophile than bromine. Why is that? Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via nucleophilic substitution. In this type of reaction, the nucleophile displaces a leaving group from a carbon atom of an organic substrate (here the alcohol once protonated). Both electrons of the new bond to the carbon are provided by the nucleophile while the...
which is the better nucleophile? cho CH₂S
can anyone help me on this? 2. (4 pts) Which is the better nucleophile, chloride or bromide ion and why? Discuss this in the context of the data and in terms of the nature of the chloride ion and the bromide ion. (4 pts) Why is the ratio of bromo to chloro products roughly even when using tert- butanol as the substrate compared to using 1-butanol as the substrate? f(2 pts) Why must the nucleophile mixture be highly acidified for...
1. why is toluene a stronger nucleophile than benzene? 2.why is phenol a stronger nucleophile than benzene?
1. why is toluene a stronger nucleophile than benzene? 2.why is phenol a stronger nucleophile than benzene?
Why is NC- a good nucleophile? and why is it a weak base?