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Carbonic acids
=O and –OH group influences each other:
• =O it does not show the properties typical of aldehydes
• -OH it dissociates much more

Carbonic acids: Numbering
Reactions of carbonic acids
Salt formation: NaOH, Na2CO3, Na
Ester formation
Decarboxylation: under the influence of heat
Strongest acid
Formic acid
Acid Strength
+ alkil-group – (e-sending prop.) → acid strength decreases
+ e- attractive group (Cl, Br) → acid strength increases
Dicarboxylic acids
one is a strong acid, the other a weak acid
Aromatic acids
Stronger
Lactic acid


Lactic acid identification: Legal reaction_Step 1


Lactic acid identification: Legal reaction_Step 2
acetaldehyde


Lactic acid identification: Legal reaction_Step 3
Sodium nitroprusside: [Fe(CN)5 NO]2-
![<p>Sodium nitroprusside: [Fe(CN)5 NO]2-</p>](https://assets.knowt.com/user-attachments/f3ef4bda-771d-4148-a0d7-2a9daf078d4a.jpg)
Lactil lactate

Dilactone


Lactic Acid Assay Step 1


Lactic Acid Assay Step 2


Lactic Acid Assay Step 3

Lactic Acid Assay Calculation

Tartaric acid


Tartaric acid Identification: Fenton reaction Step 1


Tartaric acid Identification: Fenton reaction Step 2


Tartaric acid Identification: Fenton reaction Step 3


Tartaric acid Identification: Fenton reaction Step 4

Sorbic acid

Citric acid


Citric acid Identification: dissolve in acetic anhydride + pyridine mixture

Citric acid Identification: compound + water + NaOH solution + calcium-chloride-solution → boiling → white ppt
White ppt.


DENIGES-REACTION: Citric acid Step 1
compound + water + mercury (II) sulphate solution → boiling → + 3 drops potassium permanganate → white ppt


DENIGES-REACTION: Citric acid Step 2
White ppt
