Answer:
Repeated SN2 reactions occur leading to the formation of a racemic mixture
Explanation:
S-2-iodooctane is a chiral alkyl halide with an asymmetric carbon atom. The presence of an asymmetric carbon atom implies that it can rotate plane polarized light and thus lead to optical isomerism. The two configurations of the compound are R/S according to the Cahn-Prelong-Ingold system.
However, when S-2-iodooctane is treated with sodium iodide in acetone, repeated SN2 reactions occur since the iodide ion is both a good nucleophile and a good leaving group. Hence a racemic modification is formed in the system with time hence we end up with (±)- Iodooctane.
Answer:
1.
work out the mean mode median and range
Explanation:
Tell your teacher. They'll know what to do and it's best to report it to them.
Answer:
see calculations in explanation
Explanation:
percent = part/total x 100%
part = ∑ atomic mass of element
- hydrogen = 1.008 amu (atomic mass units)
- carbon = 12.011 amu
- nitrogen = 14.007 amu
total = ∑ molecular mass of compound
= H amu + C amu + Namu
= 1.008 amu + 12.011 amu + 14.007 amu
= 27.026 amu
%H = (1.008amu/27.026amu)100% = 3.730%
%C = (12.011amu/27.026amu)100% = 44.442%
%N = (14.007amu/27.026amu)100% = 51.827%
Check results ∑%values = 100%
3.730% + 44.442% + 51.827% = 99.999% ≅ 100%
Answer:
I don't know lol laugh out loud
