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  2. Chromic acid - Wikipedia

    en.wikipedia.org/wiki/Chromic_acid

    Chromic acid in aqueous sulfuric acid and acetone is known as the Jones reagent, which will oxidize primary and secondary alcohols to carboxylic acids and ketones respectively, while rarely affecting unsaturated bonds. [12] Pyridinium chlorochromate is generated from chromium trioxide and pyridinium chloride.

  3. Bicarbonate buffer system - Wikipedia

    en.wikipedia.org/wiki/Bicarbonate_buffer_system

    k H CO 2 is a constant including the solubility of carbon dioxide in blood. k H CO 2 is approximately 0.03 (mmol/L)/mmHg; p CO 2 is the partial pressure of carbon dioxide in the blood; Combining these equations results in the following equation relating the pH of blood to the concentration of bicarbonate and the partial pressure of carbon ...

  4. Ketogenesis - Wikipedia

    en.wikipedia.org/wiki/Ketogenesis

    The accumulation of acetyl-CoA in turn produces excess ketone bodies through ketogenesis. [11] The result is a rate of ketone production higher than the rate of ketone disposal, and a decrease in blood pH. [12] In extreme cases the resulting acetone can be detected in the patient's breath as a faint, sweet odor.

  5. Carbaminohemoglobin - Wikipedia

    en.wikipedia.org/wiki/Carbaminohemoglobin

    Respiratory acidosis: This condition is characterized by a build up of carbon dioxide in the blood, which leads to a drop in the blood's pH. This occurs when there is an impairment in the gas exchange process, such as respiratory failure. [15] Hypoventilation: This type of condition can result in higher levels of carbaminohemoglobin.

  6. Ketosis - Wikipedia

    en.wikipedia.org/wiki/Ketosis

    Ketosis is a metabolic state characterized by elevated levels of ketone bodies in the blood or urine. Physiological ketosis is a normal response to low glucose availability. . In physiological ketosis, ketones in the blood are elevated above baseline levels, but the body's acid–base homeostasis is maintain

  7. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  8. I'm Taking Metformin. Could It Cause Me to Lose Hair?

    www.aol.com/im-taking-metformin-could-cause...

    Metformin is a prescription medication used to treat high blood sugar in those with type 2 diabetes who are resistant to the effects of insulin. ... the most common adverse reactions of metformin ...

  9. Bargellini reaction - Wikipedia

    en.wikipedia.org/wiki/Bargellini_reaction

    In the author's own words, "The first phase in the reaction is probably the formation of acetonechloroform--(which may, indeed, be used in place of the chloroform), this being then acted on by sodium hydroxide in presence of acetone, yielding α-hydroxyisobutyric acid, which, with the phenol, gives α-phenoxyisobutyric acid.