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Bas_tet
10 days ago
14

What assumption is being made if scientists conclude that aspartic acid was formed by the prebiological synthesis in the passage

?
A.Aspartic acid is unstable at temperatures below 150°C.
B.All of the malic acid underwent the dehydration reaction to form fumaric/maleic acid.
C.Compound A and cyanide were available on primitive Earth.
D.The reaction between ammonia and fumaric acid was catalyzed by the presence of water.
Chemistry
2 answers:
lorasvet [2.6K]10 days ago
8 0

Answer:

A....

Explanation:

alisha [2.8K]10 days ago
6 0

Answer:

A. Aspartic acid is unstable at temperatures below 150°C.

Explanation:

Aspartic acid is an amino acid utilized in protein synthesis in living organisms. It possesses an amino group and a carboxylic acid, and the body can produce it. This amino acid is classified as non-essential. It was inferred from the text that aspartic acid cannot remain stable below 150°C. The transamination process involving oxaloacetate in humans results in the production of aspartate, facilitated by the enzyme aminotransferases. Moreover, aspartate plays a significant role in urea synthesis as a metabolite.

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VMariaS [2867]

While the original inquiry is incomplete, the comprehensive question is:

Many chemicals can illustrate spots on a TLC plate that have been processed and dried. The permanganate used in the video creates yellow spots against a purplish background, taking advantage of the oxidizing capability of basic permanganate (MnO4), which outperforms chromic acid as an oxidizing agent. Chromic acid can also be employed to visualize spots, resulting in a green hue on the yellow background, indicating oxidation. So, can chromic acid be conveniently used to visualize spots when tracking a reaction converting an alcohol into a ketone? What observations are anticipated if one attempts this? Furthermore, if a small amount of alcohol is included in a solvent mixture for eluting your TLC plate, why must the plate be fully dried before visualizing the spots with an oxidizing agent like permanganate or chromic acid?

Answer:

Typically, using chromic acid to visualize spots during the conversion of alcohol to ketone is not feasible. The alcohol (substrate) will convert into its respective ketone due to the presence of chromic acid, causing the spots for the product and the reactant to align horizontally. This alignment complicates differentiation between the spots, making chromic acid unsuitable for this purpose.

It's vital to ensure that the plate is completely dry before observing spots with an oxidizing agent, even if alcohol is present in the solvent mixture. Incomplete drying could lead to oxidation of the alcohol by the oxidizing agent, resulting in transformation to carboxylic acid or ketone, thereby creating a new spot.

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1 month ago
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