Skip to main content
25 votes

Why does bleach feel slippery?

Actually it is saponification. Bleach has alkali added to it, to stabilize it against decomposion to chlorine gas. To wash your hands after contact with bleach was a wise move.
Oscar Lanzi's user avatar
  • 62.4k
24 votes
Accepted

Why does bleach feel slippery?

Maybe it needs to be clarified that the salt of a strong base and a weak acid can conduct saponification. Therefore the fact that bleach reacts with fatty acids creating soap, does not necessarily ...
Kinformationist's user avatar
8 votes

Producing soap from sodium carbonate and oil

In nature fat is stored as triglycerides (TGs): Three fatty acid (FA) chains bound together by a glycerol backbone. Olive oil is mainly composed of TGs, though it also contains small amounts of free ...
Veritas's user avatar
  • 471
5 votes
Accepted

Soap equation using potash

Ashes have been thoroughly studied more than $100$ years ago. See the Dictionnaire de chimie (in French) by A. Wurtz, Hachette ed., Paris, 1872, p. 787 - 789. Potassium hydroxyde $\ce{KOH}$ was never ...
Maurice's user avatar
  • 30k
4 votes

Soap equation using potash

Can somebody help me understand how the soap and the glycerin molecule would look like? Once you add water, you have potassium ions and hydroxide ions in solution, and the products look the same as ...
Karsten's user avatar
  • 42.3k
4 votes

Soap equation using potash

Once you introduce water, potassium carbonate can generate potassium hydroxide through the hydrolysis reaction $\ce{CO3^{2-} + H2O <=> HCO3^- +OH^-},$ and this reaction is fairly efficient ...
Oscar Lanzi's user avatar
  • 62.4k
2 votes

How strong (molarity) does NaOH solution need to be to saponify fats?

2.5 M might be a bit strong. 1.0 M is 40 g NaOH per liter of water, or around 4% solution. Start with 1 % solution and leave it soak. As with oven cleaners, a little heat should help move things ...
Robert DiGiovanni's user avatar
2 votes

Which one reacts first with NaOH; Triglycerides or FFA?

Triglycerides require nucleophilic displacement of the glycerin component, whereas FFAs require only deprotonation. The latter is much faster.
Oscar Lanzi's user avatar
  • 62.4k
1 vote
Accepted

Where do the chloride ions go during saponification precipitation?

Adding a concentrated $\ce{NaCl}$ solution to a soap solution produces the precipitation of sodium alkanoates (indeed it is a mixture of alkanoates and alkenoates). This is a consequence of the law of ...
Maurice's user avatar
  • 30k
1 vote
Accepted

Molecularity of Saponification Reaction

You should know that the molecularity is not relevant in your case and has no significance for multi-step reactions, it is just applicable to elementary reactions. The relevant parameter for multi-...
gabriel chris's user avatar
1 vote
Accepted

Gelatination of solution in saponification

Sodium stearate is not very soluble in water (above about 2%, it becomes viscous but not a firm gel). Ethanol can reduce the viscosity at first, but sodium stearate is not soluble in ethanol either, ...
James Gaidis's user avatar
  • 14.3k

Only top scored, non community-wiki answers of a minimum length are eligible