
Concept explainers
a.
To match:
The metabolic
Introduction:
Nucleotides are the building blocks of the
b.
To match:
The metabolic nucleotide that matches with the description “exchanges energy when
Introduction:
Nucleotides are the building blocks of the nucleic acids such as deoxyribo nucleic acid (DNA), and ribonucleic acid (RNA). These nucleotides have significant metabolic functions in cells, therefore, called as “metabolic nucleotides”. They act as energy exchanger and can also be coenzymes. Metabolic nucleotides have two forms: a high energy form and a low energy form.
c.
To match:
The metabolic nucleotide that matches with the description “the oxidized form of Flavin adenine dinucleotide”
Introduction:
Nucleotides are the building blocks of the nucleic acids such as deoxyribo nucleic acid (DNA), and ribonucleic acid (RNA). These nucleotides have significant metabolic functions in cells, therefore, called as “metabolic nucleotides”. They act as energy exchanger and can also be coenzymes. Metabolic nucleotides have two forms: a high energy form and a low energy form.

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Chapter 12 Solutions
EBK LABORATORY MANUAL FOR GENERAL, ORGA
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
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- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
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