Answer:
Carnitine Synthesis
Explanation:
Ascorbic acid acts as a cofactor in various hydroxylation and amidation reactions by electron transfer to enzymes that provide reducing equivalents. Accordingly, ascorbic acid is required or facilitates the conversion of certain proline and lysine residues of the procollagen, the oxidation of lysine side chains to proteins, providing hydroxytrimethylsiline for carnitine synthesis. This means that ascorbic acid is essential for the carnitine synthesis.
Carnitine is derived from amino acids and acts as a cofactor for the enzyme acetyltransferase responsible for the transport of fatty acids to mitochondria. Your presence in the body is very important for feeling energetic and strong. The lack of canitine, influenced by the lack of ascorbic acid in individuals suffering from scurvy, causes a lack of energy.
The relation between density and mass and volume is
the dose required is 2.5 tsp
each tsp contain 5mL
So dose required in mL = 2.5 X 5 = 12.5 mL
the mass will be calculated using following formula
The mass of dose in grams will be 15.38 g
Answer:
Aqueous layer (1 M HCI)
Explanation:
First of us I want to remind you of the cliché in chemistry that like dissolves like. In solvent extraction, a mixture is dissolved in a system consisting of two immiscible solvents. One layer is organic while the other layer is aqueous.
Polar substances partition in the aqueous layer while nonpolar substances partition in the organic layer.
Since Copper sulfate is ionic, we will find it in the aqueous layer according to the old chemistry cliche.
Benzaldehyde or C6H5CHO would not undergo the aldol condensation because it does not contain an alpha-hydrogen in its structure. Aldol condensation is a type of reaction that happens between an enolate and an aldehyde or ketone leading to a alkene that has a planar structure. The lack of an alpha-hydrogen would not allow for it to undergo such process since it cannot enolize. Benzaldehyde undergoes a nucleophilic reaction known as Claisen-Schmidt condensation. It has somehow same mechanism of the aldol reaction however, the nucleophilic attack on the carbonyl happens even without the alpha-hydrogen but with an enolate that is from a ketone.
Answer:
yes the one that is circled is correct
Explanation:
