rigid because of the resonance stabilization of the amide (peptide) bond and the C=O (C double bond O) cause the structure to be planar and is therefore incapable of rotation.
resonance (bond delocalization) I believe.
due to restriction caused by rotation around alpha c - n bond
It is due to sp2 hybridization and planar structure of carbonyl carbon.
Yes, a peptide bond is a covalent bond.
there is no specific length for the peptide bond, but there are million amino acids that build up a peptide bond
An amide bond forming a chain of peptides. Peptide bond is only a special amide bond name for this particular bonding.
If the peptide bond is hydrolyzed, then an H20 molecule is consumed.
Peptide bond is the bond formed between amino acids. Glycosidic bond is the bond formed between simple sugars Peptide bond is the bond formed between amino acids. Glycosidic bond is the bond formed between simple sugars
due to delocalization of the lone pair of electrons of the nitrogen onto carbonyl oxygen
This is called a peptide bond, or peptide linkage.
Yes, a peptide bond is a covalent bond.
there is no specific length for the peptide bond, but there are million amino acids that build up a peptide bond
They don't, exactly. However, both the nitrogen and the carbon participating in the bond are in the sp2 hybridization state, and this allows for a resonance structure making the group planar and restricting rotation about the carbon-nitrogen bond.
a peptide bond
An amide bond forming a chain of peptides. Peptide bond is only a special amide bond name for this particular bonding.
the bond connecting two aminoacid is peptide bond
If the peptide bond is hydrolyzed, then an H20 molecule is consumed.
A peptide bond
No, glycine is the simplest amino acid and does not have any peptide bond.
proteins; they form a covalent bond with amino acids creating a peptide bond