The lighter components are able to rise higher in the column before they are cooled to their condensing temperature, allowing them to be removed at slightly higher levels.
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Answer:
c. decarboxylation of an a-keto acid.
Explanation:
Decarboxylation refers to the removal of the carboxyl group from a carboxylic acid and thus releasing carbon dioxide. Decarboxylases are enzymes that speed up the removal of the carboxyl group from acids. These reactants could be amino acids, alpha-keto acids, and beta-keto acids. Biotin is known to catalyze the decarboxylation of malonyl CoA to acetyl CoA during fatty acid synthesis.
Malonyl CoA is converted to acetyl CoA after decarboxylation assisted by biotin also known as Vitamin H. Alpha keto acids are involved in fatty acids synthesis and Malonyl CoA is an alpha-keto acid because the keto group is located in the first carbon near the carboxylic acid group. Keto acids have both a carboxyl group and a ketone group.
Answer:
D) SrCO3(s) + 2 HNO2(aq) → Sr(NO2)2 + H2O + CO2(g)
Explanation:
When an acid react with carbonate, it produces nitrate, carbon-dioxide gas and water molecule. When nitrous acid react with Strontium carbonate, three products are formed i. e. Strontium nitrate, carbon-dioxide gas and water. In the reaction, both nitrous acid and Strontium carbonate exchange their partners with each other and forming a different products.
The correct option is (b)
NaNH2 is an effective base. It can be a good nucleophile in the few situations where its strong basicity does not have negative side effects. It is employed in elimination reactions as well as the deprotonation of weak acids.Alkynes, alcohols, and a variety of other functional groups with acidic protons, such as esters and ketones, will all be deprotonated by NaNH2, a powerful base.Alkynes are deprotonated with NaNH2 to produce what are known as "acetylide" ions. These ions are powerful nucleophiles that can react with alkyl halides to create carbon-carbon bonds and add to carbonyls in an addition reaction.Acid/base and nucleophilic substitution are the two types of reactions.Using the right base, terminal alkynes can be deprotonated to produce a carbanion.A good C is the acetylide carbanion.The acetylide carbanion can undergo nucleophilic substitution reactions because it is a potent C nucleophile. (often SN2) with 1 or 2 alkyl halides with electrophilic C to create an internal alkyne (Cl, Br, or I).Elimination is more likely to occur with 3-alkyl halides.It is possible to swap either one or both of the terminal H atoms in ethylene (acetylene) to create monosubstituted (R-C-C-H) and symmetrical (R = R') or unsymmetrical (R not equal to R') disubstituted alkynes (R-C-C-R').
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