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  2. 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.

  3. Jones oxidation - Wikipedia

    en.wikipedia.org/wiki/Jones_oxidation

    For oxidations to the aldehydes and ketones, two equivalents of chromic acid oxidize three equivalents of the alcohol: 2 HCrO 4 − + 3 RR'C(OH)H + 8 H + + 4 H 2 O → 2 [Cr(H 2 O) 6] 3+ + 3 RR'CO. For oxidation of primary alcohols to carboxylic acids, 4 equivalents of chromic acid oxidize 3 equivalents of the alcohol. The aldehyde is an ...

  4. Neutralization (chemistry) - Wikipedia

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

    For example, sodium hydroxide, NaOH, is a strong base. NaOH(aq) → Na + (aq) + OH − (aq) Therefore, when a strong acid reacts with a strong base the neutralization reaction can be written as H + + OH − → H 2 O. For example, in the reaction between hydrochloric acid and sodium hydroxide the sodium and chloride ions, Na + and Cl − take ...

  5. Sodium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydroxide

    2 Al + 2 NaOH + 2 H 2 O → 2 NaAlO 2 + 3 H 2 Sodium aluminate is an inorganic chemical that is used as an effective source of aluminium hydroxide for many industrial and technical applications. Pure sodium aluminate (anhydrous) is a white crystalline solid having a formula variously given as NaAlO 2 , Na 3 AlO 3 , Na[Al(OH) 4 ] , Na 2 O·Al 2 ...

  6. Sodium ethoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_ethoxide

    Sodium ethoxide, also referred to as sodium ethanolate, is the ionic, organic compound with the formula CH 3 CH 2 ONa, C 2 H 5 O Na, or NaOEt (Et = ethyl). It is a white solid, although impure samples appear yellow or brown. It dissolves in polar solvents such as ethanol. It is commonly used as a strong base. [2]

  7. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    The Group 1 metal (M) is oxidised to its metal ions, and water is reduced to hydrogen gas (H 2) and hydroxide ion (OH −), giving a general equation of: 2 M(s) + 2 H 2 O(l) 2 M + (aq) + 2 OH − (aq) + H 2 (g) [8] The Group 1 metals or alkali metals become more reactive as their number of energy levels inceases.

  8. Alcohol (chemistry) - Wikipedia

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

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  9. Hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrolysis

    M(H 2 O) n m+ + H 2 O ⇌ M(H 2 O) n−1 (OH) (m−1)+ + H 3 O + Thus the aqua cations behave as acids in terms of Brønsted–Lowry acid–base theory . This effect is easily explained by considering the inductive effect of the positively charged metal ion, which weakens the O−H bond of an attached water molecule, making the liberation of a ...

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