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When both nh2 and COOH replace hydrogen atoms on the same carbon what is formed?
it forms an amino acid
When both NH2 and COOH replace hydrogen atoms on the same carbon atom?
... then you get an (alpha)amino acid: NH2CH2COOH glycine
How to reduce phenylalanine with thionylchloride what is the proper solvant so I can end up with the cooh being replaced with cl. And can I use LAH to replace the CL with Hydrogen the formula?
What solvant can I use with thionylchloride + phenylalanine for reduction of the COOH so it is replaced with CL? And can I use LAH to remove the CL to replace it with Hydrogen ? And can I use MEOH to attach a CH3 after this? Would you please help me with these questions and write the mole formula for this with the temp.
What combination of atoms makes the molecule of stearic acid an acid?
The acidic nature of stearic acid is due to the presence of a carboxylic acid functional group (-COOH). This group is composed of one carbon atom, one oxygen atom, and one hydrogen atom. The hydrogen atom within the carboxylic acid group can ionize to release a proton, leading to its acidic behavior.
What is formed when a COOH is substituted for three hydrogen atoms attached to the same carbon atom?
A carboxylic acid group (-COOH) is formed when a COOH group is substituted for three hydrogen atoms attached to the same carbon atom. It consists of a carbonyl group (C=O) and a hydroxyl group (OH) attached to the same carbon atom. This functional group is commonly found in organic compounds like acetic acid.
When both nh2 and COOH replace hydrogen atoms on the same carbon what is formed?
it forms an amino acid
When both -NH2 and -COOH replace hydrogen atoms on the same carbon atom and what is formed?
When both -NH2 and -COOH replace hydrogen atoms on the same carbon atom, an amino acid is formed.
When both NH2 and COOH replace hydrogen atoms on the same carbon atom?
... then you get an (alpha)amino acid: NH2CH2COOH glycine
When both NH2 and COOH replace hydrogen atoms on the same carbon atom a(n) is formed.?
These substances are called aminoacids.
When a -COOH group replaces a hydrogen in a hydrocarbon the result is?
An Alcohol.
How to reduce phenylalanine with thionylchloride what is the proper solvant so I can end up with the cooh being replaced with cl. And can I use LAH to replace the CL with Hydrogen the formula?
What solvant can I use with thionylchloride + phenylalanine for reduction of the COOH so it is replaced with CL? And can I use LAH to remove the CL to replace it with Hydrogen ? And can I use MEOH to attach a CH3 after this? Would you please help me with these questions and write the mole formula for this with the temp.
Why is phosphoric acid an acid and it does not contain the carboxyl group -cooh?
Phosphoric Acid is an acid because it dissociates into Hydrogen and phosphate ions. Second Question. COOH- doesn't make something an acid. It makes it an acetate. Acetate is part of a weak acid, Acetic Acid.
Why hydrogen of COOH group is removed in preparation of methy salicylate from salicylic acid in the presence of sulphuric acid?
why hydrogen of COOH group is removed in the preparation of methyl salicylate from salicylic acid in the presence of sulphuric acid
What combination of atoms makes the molecule of stearic acid an acid?
The acidic nature of stearic acid is due to the presence of a carboxylic acid functional group (-COOH). This group is composed of one carbon atom, one oxygen atom, and one hydrogen atom. The hydrogen atom within the carboxylic acid group can ionize to release a proton, leading to its acidic behavior.
What is r-cooh?
R = aryl or alkyl group. O = Oxygen, C = Carbon, H = Hydrogen. With that said: R-COOH Indicates an aryl/alkyl bound to a carbon, bound to two oxygens and one oxygen is bound to a hydrogen. If you complete their valence shells you get. R-C=O | O-H
Which part of a fatty acid is hydrophobic?
the tail ( carbon hydrogen only part) the COOH part that makes it an acid does engage in hydrogen bonding.
How many ionisable hydrogen atoms are there in acetic acid?
There is one ionizable hydrogen atom in acetic acid. This hydrogen atom is located on the carboxyl group (COOH) of the molecule and can dissociate to form a hydrogen ion (H+) in solution.
