(1) All compounds which are more acidic than water can be dissolved in aqueous NaOH, like Phenol, Carboxylic acid etc. Alcohols in general are not soluble in NaOH.

(2) When primary and secondary alkyl halides (R-X) are reacted with aqueous NaOH (or KOH) alcohols (R-OH) are formed (By substitution SN2 because OH is considered to be a strong nucleophile) and small quantity of alkene is also formed. Tertiary alkyl halides give almost alkene as product (By elimination E2 reaction). Since SN2 reaction so if in R-X the carbon which is attached with -X (the leaving group) is chiral the inversion takes place called Walden inversion. For SN2 the reactivity for compounds like RCOCH2Cl is very high, for compounds like ROCH2Cl reactivity is high, for compounds like C6H5CH2Cl and CH3Cl the reactivity is very good then other compounds like allyl halide CH2=CH2-CH2-Cl and then primary alkyl halides. SN2 reactivity is very poor for compounds like phenyl halide C6H5-Cl, compounds where L.G is attached at bridge head carbon, tertiary alkyl halides, primary but crowded at beta carbon.

(3) When alkyl halides are boiled with ethanolic NaOH or KOH alkenes are obtained. During the elimination here one H (electrofugal atom) and one halogen (nucleofugal atom) leaves. The two leaves with antiperiplanar geometry. The reaction is regioselective in forming more substituted stable product as major product (Saytzeff’s or Zaitsev’s rule). Hofmann product as minor product (less substituted alkene).   

(4) NaOH/X2 is an important reagent to test methyl aldehyde or methyl ketone. X2 can be Cl2, Br2 or I2. After the reaction we get a carboxylate salt and haloform. When the reaction is carried out using NaOH and I2, iodoform is obtained as yellow crystalline solid. The test is called iodoform test. NaOX can also be used in place of NaOH + X2. The haloform test is given aldehydes or ketones having CH3CO- group or alcohols having CH3CHOH- group. Other bonds like C-C double and triple bonds remain unaffected. Same reagent NaOH (or KOH) + Br2 (or Cl2) can be used for the conversion of primary amides (RCONH2) into primary amines containing one carbon atom less than the number of carbon atoms present in the amide (Hofmann bromamide, rearrangement  or degradation reaction). This Hofmann bromamide reaction can only be given by amides in which two H atoms are present with N, possible intermediates which have been isolated are RCONHBr, [RCONBr], RNCO. Please note in RCONH2, R can be alkyl or aryl but if alkyl of more than 7 carbon atoms then yield is low and mainly alkylcyanide RCN is produced. Side reactions in this bromamide reaction is where ureas (RNHCONHR) or acylureas (RCONHCONHR) are obtained by the addition of RNH2 and RCONH2 with intermediate alkylisocyanate RNC. A similar reaction where RCONH2 is treated with Pb(OAc)4 first RNCO forms which gets converted into RNHCONHR or if RNCO is reacted with R-OH then NaOH RNH2 forms.

(5) Aldehydes and ketones that contain at least one alpha H atom undergo dimerization in the presence of dilute NaOH (or KOH or Na2CO3 or acid) to form beta-hydroxyaldehdes and beta-hydroxyketones respectively. These are called aldols and process is aldol addition. When the aldol is heated in presence of an acid it undergoes dehydration and gives alpha-beta-unsaturated aldehydes or ketones. If two different aldehydes and ketones are used reaction is called crossed aldol condensation. In crossed aldol condensation if one component is aromatic aldehyde then reaction is called Claisen reaction. If in place of aldehydes and ketones two esters are used for condensation reaction with base like RONa then beta keto ester forms as product and sometimes this reaction is referred as Claisen condensation and if two esters are present in the same compound intra molecular condensation may take place called Dickmann condensation (used for formation of 5,6,7 membered rings).

(6) Aldehydes that do not have alpha hydrogen atom undergo self-oxidation and self-reduction (disproportionation) on heating with concentrated NaOH. One molecule gets reduced to alcohol and another molecule gets oxidised to salt of carboxylic acid. There are few exceptions in this like isobutyraldehyde(alpha-monoalkylated aldehydes) although possesses alpha H but undergoes Cannizzaro reaction. A trihaloacetaldehyde does not have alpha H but does not undergo Cannizzaro reaction instead undergoes nucleophilic substitution of -CX3 by -OH (from NaOH) to give haloform and sodium formate. If two different aldehydes or ketones are used in the reaction it is called crossed Cannizzaro reaction. If formaldehyde (HCHO) is present in crossed Cannizzaro reaction HCHO undergoes oxidation. If the concentration of NaOH in the reaction is very high the order of the reaction will be 4 (Order 2 with respect to Aldehyde and order 2 with respect to NaOH) and if the concentration of NaOH is not very high then overall order will be 3 (Order 2 with respect to aldehyde and 1 with respect to NaOH). Reaction involves transfer of hydride from one aldehyde to another molecule (Rate determining) so even if solution has D2O formed alcohol does not contain any alpha-deuterium.

(7) When sodium or potassium salt of carboxylic acid is heated with soda-lime (NaOH + CaO) undergoes decarboxylation (CO2 liberates) to form alkane which has one carbon less than the starting carboxylate salt. Reaction follows carbanion mechanism. Another method for getting alkane using decarboxylation is ELECTROLYTIC DECARBOXYLATION also known as Kolbe’s reaction (when sodium or potassium salt of carboxylic acid (2RCOONa) is electrolysed in water, DMF or methanol using platinum electrodes we get an alkane R-R. Please note there are carboxylic acids (if alpha carbon has resonance electron withdrawing group such as >C=O, -CN, -NO2, >C=C<, -COOH which on simply heating undergo decarboxylation by liberating CO2.

(8) Kolbe Schmitt Reaction: When sodium phenoxide is treated with CO2 gas at around 125oC and 4 to 7 atm pressure sodium salicylate is formed as the major product which on acidification gives salicylic acid.