bond cleavage वाक्य
उदाहरण वाक्य
मोबाइल
- Bond cleavage is also possible by a process called homolysis.
- Glucansucrase uses the energy released from bond cleavage to drive glucan synthesis.
- Bond cleavage of imine to acetal by action of ethanol
- The formation of AB + requires bond cleavage without the offsetting bond formation.
- Electrons delocalized in the carbon-carbon bond cleavage associate with the alcohol group.
- Note that water is required for normal peptide bond cleavage of the iminolactone intermediate.
- The active site comprises five highly conserved motifs that collectively catalyze glycosidic bond cleavage:
- Heterolytic bond cleavage and heterolytic substitution reactions can result in the formation of ion pairs.
- After isomerization, a conjugation of the polyene chain and completes the ester bond cleavage.
- Stemmadenine is believed to be formed from preakuammicine by a carbon-carbon bond cleavage.
- Glycosidic bond cleavage produces short cellulose chains of two-to-seven monomers comprising the melt.
- This type of compounds undergoes bond cleavage and bond creation upon irradiation with particular wavelengths of light.
- NHC formation typically occurs by heterolytic bond cleavage, so small, coordinating anions favor this pathway.
- The peptide bond cleavage occurs via the nucleophilic attack of water at the carbonyl between two adjacent amino acid residues.
- Its important to note that the fourth reaction in the series is an inverted homolytic bond cleavage stated in terms of free energy.
- The double bond serves as the target of oxidation and carbon-to-carbon bond cleavage, thereby shortening the fatty acid chain.
- N-O bond cleavage of the Barton ester can also occur spontaneously upon heating or by irradiation with light to initiate the reaction.
- Even reactions that involve only bond cleavage from the carbon, such as S N 1 reactions, involve strengthening of the remaining bonds to carbon.
- ""'Bgl " II "'catalyses phosphodiester bond cleavage at the DNA backbone through a phosphoryl transfer to water.
- However, the currently accepted mechanism involves a rapid four-electron reduction involving immediate oxygen-oxygen bond cleavage, avoiding any intermediate likely to form superoxide.
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