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Solubility Like dissolves like Organic compounds are not expected to be soluble in water Rule of Thumb: C/O ratio.

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Presentation on theme: "Solubility Like dissolves like Organic compounds are not expected to be soluble in water Rule of Thumb: C/O ratio."— Presentation transcript:

1 Solubility Like dissolves like Organic compounds are not expected to be soluble in water Rule of Thumb: C/O ratio

2 However, If the organic compound can be ionized It is more likely to be water-soluble Requirement: the presence of an ionizable atom/group since ionic compounds are polar, and thus water-soluble What is an ionizable atom/group one which can form a conjugate acid or conjugate base upon treatment with an acid or base

3 Classification of Organic Compounds from a solubility point of view will be soluble upon reaction with Examples basicacid (HCl –aq)Amines weakly acidicstrong base (NaOH –aq)Phenols strongly acidicweak base (NaHCO 3 –aq)Carboxylic Acids neutralstrong acid (H 2 SO 4 –conc)Alcohols, Aldehydes, Ketones, Esters, etc inertalways insolubleNo ionizable FG e.g. alkyl halides

4 will be soluble upon reaction with Examples basicacid (HCl –aq)Amines

5 will be soluble upon reaction with Examples weakly acidicstrong base (NaOH –aq)Phenols

6 phenolate But

7 Phenols have very different acid-base properties compared to alcohols phenolate a phenolate, the conjugate base of a phenol, is much more stable than an alkoxide alkoxide the conjugate base of an alcohol

8 extensive charge delocalization into the aromatic ring no charge delocalization here

9 extensive charge delocalization into the aromatic ring electron/charge delocalization is a stabilizing factor more stable weaker conjugate base the conjugate base of a stronger acid is a weaker conjugate base thus a phenols is a stronger acid than an alcohol

10 will be soluble upon reaction with Examples strongly acidicweak base (NaHCO 3 –aq)Carboxylic Acids

11 will be soluble upon reaction with Examples neutralstrong acid (H 2 SO 4 –conc)Alcohols, Aldehydes, Ketones, Esters, etc all insoluble with water if C/O ratio > 4 not strongly basic enough to ionize in the presence of NaOH (aq) ( remember why not ) But oxygen will protonate upon treatment with H 2 SO 4 (conc)

12 will be soluble upon reaction with Examples neutralstrong acid (H 2 SO 4 –conc)Alcohols, Aldehydes, Ketones, Esters, etc

13 will be soluble upon reaction with Examples inertalways insolubleNo ionizable FG e.g. alkyl halides

14 Samples to be tested N-ethylaniline  -naphthol (a phenol) benzoic acid butanol para -dichlorobenzene


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