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  2. 4-Chlorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Chlorobenzaldehyde

    It can be produced by hydrolysis of 4-chlorobenzal chloride: [2]. ClC 5 H 4 CHCl 2 + H 2 O → ClC 5 H 4 CHO + 2 HCl. It can also be produced by the oxidation of 4-chlorobenzyl alcohol.

  3. File:Male Masturbation with Ejaculation Video.webm - Wikipedia

    en.wikipedia.org/wiki/File:Male_Masturbation...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  4. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.

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  6. Benzal chloride - Wikipedia

    en.wikipedia.org/wiki/Benzal_chloride

    Benzal chloride is an organic compound with the formula C 6 H 5 CHCl 2. [1] This colourless liquid is a lachrymator and is used as a building block in organic synthesis . Preparation and usage

  7. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Industrially, benzyl chloride is the precursor to benzyl esters, which are used as plasticizers, flavorants, and perfumes. Phenylacetic acid, a precursor to pharmaceuticals, is produced from benzyl cyanide, which in turn is generated by treatment of benzyl chloride with sodium cyanide.

  8. 22 Ways Men Can Make Their Orgasms Better - AOL

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    16) Use lube. Research conducted by Indiana University's Center for Sexual Health showed that using lube makes it 50% easier for both men and women to orgasm. And it makes sense, too: according to ...

  9. 2,4,6-Trichlorobenzoyl chloride - Wikipedia

    en.wikipedia.org/.../2,4,6-Trichlorobenzoyl_chloride

    It is the primary reactant in Yamaguchi esterification. 2,4,6-Trichlorobenzoyl chloride readily reacts with alcohols. This newly formed reagent, when mixed with a stoichiometric amount of 4-dimethylaminopyridine, cyclizes and forms esters. This reaction creates 2,4,6-trichlorobenzoic acid as a byproduct.