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This chemical reaction mechanism drawing depicts steps of carbonyl compound halogenation reaction.
"Alpha-substitution reactions occur at the position next to the carbonyl group, the α-position, and involve the substitution of an α hydrogen atom by an electrophile, E, through either an enol or enolate ion intermediate. ...
Alpha Halogenation of Aldehydes and Ketones.
A particularly common α-substitution reaction in the laboratory is the halogenation of aldehydes and ketones at their α positions by reaction Cl2, Br2 or I2 in acidic solution. Bromine in acetic acid solvent is often used. ...
The halogenation is a typical α-substitution reaction that proceeds by acid catalyzed formation of an enol intermediate." [Carbonyl Alpha-Substitution Reactions. Wikipedia]
This example was redesigned from the Wikimedia Commons file: Halogenierung Mechanismus Version 3-Seite001.svg. [commons.wikimedia.org/ wiki/ File:Halogenierung_ Mechanismus_ Version_ 3-Seite001.svg]
This image is available under the Creative Commons Attribution-ShareAlike 3.0 Unported License. [creativecommons.org/ licenses/ by-sa/ 3.0/ ]
The chemical drawing example "Carbonyl compound halogenation mechanism" was created using the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Alpha halogenation of aldehydes and ketones
Alpha halogenation of aldehydes and ketones, reaction arrows, reversible reaction, plus, minus, hydrogen, H, bond, covalent bond, double bond,
"Carbohydrate catabolism is the breakdown of carbohydrates into smaller units. Carbohydrates literally undergo combustion to retrieve the large amounts of energy in their bonds. Energy is secured by mitochondria in the form of ATP.
There are several different types of carbohydrates: polysaccharides (e.g., starch, amylopectin, glycogen, cellulose), monosaccharides (e.g., glucose, galactose, fructose, ribose) and the disaccharides (e.g., maltose, lactose).
Glucose reacts with oxygen in the following redox reaction, C6H12O6 + 6O2 → 6CO2 + 6H2O, the carbon dioxide and water is a waste product and the chemical reaction is exothermic.
The breakdown of glucose into energy in the form of molecules of ATP is therefore one of the most important biochemical pathways found in living organisms." [Carbohydrate catabolism. Wikipedia]
This glucose catabolism pathways map shows glycolysis by orange color, Entner-Doudoroff phosphorylating pathway by green color, Entner-Doudoroff non-phosphorylating pathway by Yellow color.
This methabolic pathway map was redesigned from Wikimedia file: Glucose catabolism pathways.svg. [commons.wikimedia.org/ wiki/ File:Glucose_ catabolism_ pathways.svg]
The biochemical diagram example "Glucose catabolism pathways map" was created using the ConceptDraw PRO diagramming and vector drawing software extended with the Biology solution from the Science and Education area of ConceptDraw Solution Park.
Catabolic pathway map
Catabolic pathway map, pyruvic acid, pyruvate, phosphoenolpyruvic acid, PEP, phosphoenolpyruvate, lactic acid, lactate, milk acid, glycolysis, glycerate, glyceric acid, glyceraldehyde, glyceric aldehyde
, glyceraldehyde 3-phosphate, triose phosphate, 3-phosphoglyceraldehyde, G3P, GADP, GAP, TP, GALP, PGAL, glucose, D-glucose, dextrose, grape sugar, glucose 6-phosphate, Robison ester, gluconolactone, ghlucono delta-lactone, GDL, gluconic acid, gluconate, fructose 6-phosphate, fructose 1,6-bisphosphate, Harden-Young ester, dihydroxyacetone phosphate, DHAP, glycerone phosphate, acetyl coenzyme A, acetyl-CoA, acetic acid, acetate, ethanoic acid, Entner-Doudoroff pathway phosphorylating, Entner-Doudoroff pathway non-phosphorylating
, 6-phosphogluconolactone, 6-phosphoglucono-δ-lactone, 6-phosphogluconic acid, 6-phosphogluconate, 3-phosphoglyceric acid, 3PG, glycerate 3-phosphate, GP, 2-phosphoglyceric acid, 2PG, 2-phosphoglycerate, 2-keto-3-deoxygluconate, KDG, 2-dehydro-3-deoxy-D-gluconate,  2-keto-3-deoxy-D-gluconic acid, 2-keto-3-deoxy-D-gluconate, 3-deoxy-2-oxo-D-gluconate, 2-keto-3-deoxygluconate, 3-deoxy-D-erythro-hex-2-ulosonic acid, 2-keto-3-deoxy-6-phosphogluconate, KDPG, 13-bisphosphoglyceric acid, 13-bisphosphoglycerate, 13BPG,