Answer:
(2R,3S)-2-ethoxy-3-methylpentane
and
(2S,3S)-2-ethoxy-3-methylpentane
Explanation:
For this case, we will have 
as nucleophile. Also, this compound is also in excess. So, we will have as solvent 
a protic solvent. Therefore the Sn1 reaction would be favored.
The first step would be the carbocation formation followed by the attack of the nucleophile. In this case both isomers would be produced: R and S (see figure).
Number 1 is incorrect, the genotypes are given to you. You need to use GG and gg. The outcome would be 100% Gg.
Number 2 is incorrect, the genotypes are given to you. You need to use Gg and Gg. The outcome would be 25% gg, 25% GG, and 50% Gg.
Number 3 is incorrect, the genotypes are given to you. You need to use TT and tt. The outcome would be 100% Tt.
Number 4 is incorrect, the genotypes are given to you. You need to use RR and rr. The outcome would be 100% Rr.
Please read the directions and use the genotypes they give you! The information is all there for you, you just need to put it in correctly. If you're still having trouble understanding how to do this, feel free to message me and I'd be happy to help you.
First, you need to know 1 kg = 10^3 g. And 1 m^3 = 10^6 m^3. So the 1 g/cm3 = 10^3 kg/m3. So the answer is 1.93*10^4 kg/m3.
<span> 2 hydrogen atoms attached to an oxygen atom.</span>
Answer: C
Explanation:
The one closest to the atomic center, there is a single 1s orbital that can hold 2 electrons. At the next energy level, there are four orbitals.
