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  2. Oxford, Cambridge and RSA Examinations - Wikipedia

    en.wikipedia.org/wiki/Oxford,_Cambridge_and_RSA...

    Oxford, Cambridge and RSA Examinations [2] (OCR) is an examination board which sets examinations and awards qualifications (including GCSEs and A-levels). It is one of England, Wales and Northern Ireland's five main examination boards. OCR is based in Cambridge, with an office in Bourn, Coventry.

  3. Lucas' reagent - Wikipedia

    en.wikipedia.org/wiki/Lucas'_reagent

    Lucas test: negative (left) with ethanol and positive with t-butanol "Lucas' reagent" is a solution of anhydrous zinc chloride in concentrated hydrochloric acid.This solution is used to classify alcohols of low molecular weight.

  4. Alcohol (chemistry) - Wikipedia

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

    In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [3] [4] Alcohols range from the simple, like methanol and ethanol, to complex, like sugars and cholesterol. The presence of an OH group strongly modifies the ...

  5. Cosolvent - Wikipedia

    en.wikipedia.org/wiki/Cosolvent

    In chemistry, cosolvents are substances added to a primary solvent in small amounts to increase the solubility of a poorly-soluble compound. Their use is most prevalent in chemical and biological research relating to pharmaceuticals and food science, where alcohols are frequently used as cosolvents in water (often less than 5% by volume [ 1 ...

  6. Oxidation with chromium(VI) complexes - Wikipedia

    en.wikipedia.org/wiki/Oxidation_with_chromium(VI...

    Cr(VI)-pyridine and pyridinium reagents have the advantage that they are soluble in organic solvents as are the alcohol substrates. One family of reagents employs the complex CrO 3 (pyridine) 2. [2] Sarett's reagent: a solution of CrO 3 (pyridine) 2 in pyridine. It was popularized for selective oxidation of primary and secondary alcohols to ...

  7. Henry reaction - Wikipedia

    en.wikipedia.org/wiki/Henry_reaction

    The Henry reaction is a classic carbon–carbon bond formation reaction in organic chemistry.Discovered in 1895 by the Belgian chemist Louis Henry (1834–1913), it is the combination of a nitroalkane and an aldehyde or ketone in the presence of a base to form β-nitro alcohols.

  8. AOL Mail

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    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. Anhydrous - Wikipedia

    en.wikipedia.org/wiki/Anhydrous

    Many processes in chemistry can be impeded by the presence of water; therefore, it is important that water-free reagents and techniques are used. In practice, however, it is very difficult to achieve perfect dryness; anhydrous compounds gradually absorb water from the atmosphere so they must be stored carefully.

  1. Related searches a level chemistry ocr alcohols and organic products solutions 5th grade

    primary alcohol formulaschemical properties of alcohol