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  2. Strecker degradation - Wikipedia

    en.wikipedia.org/wiki/Strecker_degradation

    The Strecker degradation is a chemical reaction which converts an α-amino acid into an aldehyde containing the side chain, by way of an imine intermediate. It is named after Adolph Strecker, a German chemist. The original observation by Strecker involved the use of alloxan as the oxidant in the first step, [1] followed by hydrolysis:

  3. Food chemistry - Wikipedia

    en.wikipedia.org/wiki/Food_chemistry

    The scientific approach to food and nutrition arose with attention to agricultural chemistry in the works of J. G. Wallerius, Humphry Davy, and others.For example, Davy published Elements of Agricultural Chemistry, in a Course of Lectures for the Board of Agriculture (1813) in the United Kingdom which would serve as a foundation for the profession worldwide, going into a fifth edition.

  4. Surface chemistry of cooking - Wikipedia

    en.wikipedia.org/wiki/Surface_chemistry_of_cooking

    This reaction is responsible for why meat, and many other food products, turn brown when cooked. This reaction only occurs at high temperatures. Water vapor is a byproduct of the Maillard reaction. The water molecules create a physical barrier between the proteins on the surface of the meat and the triglyceride molecules in the oil.

  5. Game day prep: 22 tailgate slow cooker dishes ranked from ...

    www.aol.com/game-day-prep-22-tailgate-163000096.html

    Slow Cooker Tailgate Recipes Ranked from Healthiest to Unhealthiest. Find the recipes here. 1. Outrageous Warm Chicken Nacho Dip. 2. Rachael's Superheated Cajun Boiled Peanuts

  6. List of reagent testing color charts - Wikipedia

    en.wikipedia.org/wiki/List_of_reagent_testing...

    It is advised to check the references for photos of reaction results. [1] Reagent testers might show the colour of the desired substance while not showing a different colour for a more dangerous additive. [ 2 ]

  7. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The reaction usually requires a catalyst, such as concentrated sulfuric acid: R−OH + R'−CO 2 H → R'−CO 2 R + H 2 O. Other types of ester are prepared in a similar manner−for example, tosyl (tosylate) esters are made by reaction of the alcohol with 4-toluenesulfonyl chloride in pyridine.

  8. Methional - Wikipedia

    en.wikipedia.org/wiki/Methional

    Methional is an organic compound with the formula CH 3 SCH 2 CH 2 CHO. It is a colorless liquid that is a degradation product of methionine.It is a notable flavor in potato-based snacks, namely potato chips, one of the most popular foods containing methional. [1]

  9. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    Formaldehyde (/ f ɔːr ˈ m æ l d ɪ h aɪ d / ⓘ for-MAL-di-hide, US also / f ə r-/ ⓘ fər-) (systematic name methanal) is an organic compound with the chemical formula CH 2 O and structure H−CHO, more precisely H 2 C=O.