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How amino acids form peptide bonds (peptide linkages) through a condensation reaction (dehydration synthesis). How amino acids form peptide bonds (peptide linkages) through a condensation reaction (dehydration synthesis). ... Peptide bond formation. This is the currently selected item.


A condensation reaction is a class of organic addition reaction that typically proceeds in a step-wise fashion to produce the addition product, usually in equilibrium, and a water molecule (hence named condensation).The reaction may otherwise involve the functional groups of the molecule, and formation of a small molecule such as ammonia, ethanol, or acetic acid instead of water.


The Mannich reaction is an example of nucleophilic addition of an amine to a carbonyl group followed by dehydration to the Schiff base.The Schiff base is an electrophile which reacts in the second step in an electrophilic addition with a compound containing an acidic proton (which is, or had become an enol). The Mannich reaction is also considered a condensation reaction.


An example is the Dieckmann condensation, in which the two ester groups of a single diester molecule react with each other to lose a small alcohol molecule and form a β-ketoester product. Many condensation reactions follow a nucleophilic acyl substitution or an aldol condensation reaction mechanism (see previous concept for more information).


10 videos Play all Amino Acids for MCAT/Biochem Students Leah4sciMCAT Empirical Formula vs Molecular Formula Calculations for the MCAT - Duration: 13:24. Leah4sciMCAT 2,632 views


MECHANISM OF THE NINHYDRIN REACTION The detection and the quantitative estimation of a-amino acids (I) has long been accomplished by their reaction with ninhydrin (If) (2,2-dihydroxy-l,3,-indandione). The reaction products include an aldehyde with one carbon atom less than the a-amino acid and ... Condensation of this


A condensation reaction occurs when two molecules join to form a larger molecule and release a smaller molecule(s) in the process. The smaller molecule lost in the reaction is often water, but it can also be methanol, hydrogen chloride, acetic acid or several other molecules.Condensation reactions occur naturally in biological and chemical processes on Earth or synthetically by man-made means.


Mechanism of the Strecker Synthesis. The reaction is promoted by acid, and HCN must be supplied or generated in situ from cyanide salts - in the latter case, one equivalent of acid is consumed in the reaction.. The first step is probably the condensation of ammonia with the aldehyde to form an imine:


Part 7: The Mechanism of Condensation Polymerization. You know that monomers that are joined by condensation polymerization have two functional groups. You also know (from Part 6) that a carboxylic acid and an amine can form an amide linkage, jand a carboxylic acid and an alcohol can form an ester linkage.