For each of the six biological polymers listed, indicate which of the properties apply. each polymer has multiple properties, an
d a given property may be used more than once. part a cellulose select all that apply. select all that apply. branched-chain polymer extracellular location glycosidic bonds informational macromolecule peptide bond β linkage phosphodiester bridge nucleoside monophosphates helical structure possible synthesis requires a template
1) Cellulose - extracellular location, glycosidic bond, β-linkage. Cellulose is polysaccharide composed of glucose linked with β-1,4 bons. 2) Messenger RNA - informational macromolecule, phosphodiester bridge, helical structure possible, synthesis requires a template. mRNA is nucleic acid, <span> mRNA is </span>translated<span> into a polymer of amino acids.</span><span> 3) </span>Globular protein - peptide bond, helical structure possible, synthesis requires a template. Protein is composed of amino acid linked with peptide bond, secundary structure can be α-helix, gene expression.<span> 4) </span>Amylopectin - branched-chain polymer, glycosidic bond, helical structure possible. Amylopectin is subunit of starch, sugar with α-1,4 and α-1,6 glycosidic bonds.<span> 5) DNA - i</span>nformational macromolecule, phosphodiester bridge, helical structure possible, synthesis requires a template, nucleoside triphosphate. DNA is helical <span>chain of </span>nucleotides<span> carrying the </span>genetic<span> instructions.</span> 6) Fibrous protein - peptide bond, helical structure possible. Protein is composed of amino acid linked with peptide bond
A triple covalent bond because each atom requires three more electrons to complete its octet.
<h3><u>Explanation</u>;</h3>
A triple covalent bond is a covalent bond formed by atoms that share three pairs of electrons.
For example;<em><u> in a diatomic molecule such a nitrogen; A nitrogen atom has five valence electrons, which can be shown as one pair and three single electrons. </u></em>When combining with another nitrogen atom to form a diatomic molecule, the three single electrons on each atom combine to form three shared pairs of electrons.
In diaxial conformation of cis-1,3-disubstituted cyclohexane, 4 gauche-butane interactions along with syn-diaxial interaction are present. Hence it readily gets converted to diequitorial conformation where no such gauche-butane interaction is present
In two possible conformations of trans-1,3-disubstituted cyclohexane, 2 gauche-butane interactions are present in each of them.
Hence cis-1,3-disubstituted cyclohexane exists almost exclusively in diequitorial form. But trans-1,3-disubstituted cyclohexane has no such option.
Trans-1,3-disubstituted cyclohexane experiences gauche butane interaction in each of the two conformations.
Therefore cis-1,3-disubstituted cyclohexane is more stable than trans conformation