Answer:
(4) option is correct
Explanation:
Given that,
The conformation of 2-methyl-3-pentanol, as viewed along the C₂-C₃ bond.
We need to find the Newman structures
Using given structures
The structure of 2- methyl-3- pentanol is shown in figure.
Through C₂-C₃ carbon shown the structure of Newman projection in figure.
Here, carbon 2 is in front side and carbon 3 is in back side in the figure.
Hence, (4) option is correct.
Answer:
Proteins and nucleic acids
Explanation:
Nitrogen compounds in animals that are no longer of use, or are in access are excreted from the animals body, and are thus called nitrogenous waste. These nitrogenous waste can be excreted in three different ways.
1. Ammonia
2. Urea
3. Uric acid
Answer:
Explanation:
you would have to look more around the page, for example look at some ways that you can right down.
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.
