the product is the AcO group (ch3-co-oh) replaces the chlorine so you have a benzene ring with a c double bond o, the carbon is then bonded to the o of the AcO group then you have another carbon=O then ch3
The reaction between acetyl chloride and sodium acetate would likely result in the formation of acetic anhydride and sodium chloride. Acetyl chloride would react with the sodium acetate to form acetic anhydride, along with sodium chloride as a byproduct.
No, sodium chloride is not soluble in ethyl acetate. Ethyl acetate is a nonpolar solvent, while sodium chloride is an ionic compound that is highly soluble in water but not in nonpolar solvents like ethyl acetate.
Ionic precipitation reaction:2Na+(aq) + S2-(aq) + Pb2+(aq)+ 2(-OOCCH3)aq --> PbS2(s) + (2Na+(aq) + 2(-OOCCH3)aq)
The reaction between calcium acetate and sodium carbonate will produce calcium carbonate and sodium acetate. This is a double displacement reaction where the cations and anions switch partners.
NO REACTION 2NaC2H3O2 + CuSO4 --> Na2SO4 + Cu(C2H3O2)2 since the two products are aqueous, this reaction does not exist
The reaction between acetyl chloride and sodium acetate would likely result in the formation of acetic anhydride and sodium chloride. Acetyl chloride would react with the sodium acetate to form acetic anhydride, along with sodium chloride as a byproduct.
To synthesize benzonitrile from benzoyl chloride, you can perform a nucleophilic substitution reaction using sodium cyanide (NaCN). In this reaction, the cyanide ion acts as a nucleophile, attacking the carbonyl carbon of benzoyl chloride, leading to the formation of benzonitrile after the elimination of hydrochloric acid (HCl). The overall reaction can be summarized as: benzoyl chloride + NaCN → benzonitrile + NaCl + HCl.
When sodium acetate is added to hydrochloric acid, the resulting precipitate will be sodium chloride. This is due to the reaction between the sodium ions from sodium acetate and the chloride ions from hydrochloric acid.
When acetic acid and sodium chloride are combined, a chemical reaction occurs where the acetic acid reacts with the sodium chloride to form sodium acetate and hydrochloric acid.
When CH3COONa reacts with HCl, it forms acetic acid (CH3COOH) and sodium chloride (NaCl). This reaction is a neutralization reaction where the sodium acetate reacts with the hydrochloric acid to produce acetic acid and sodium chloride.
No, sodium chloride is not soluble in ethyl acetate. Ethyl acetate is a nonpolar solvent, while sodium chloride is an ionic compound that is highly soluble in water but not in nonpolar solvents like ethyl acetate.
Sodium acetate is typically produced by the reaction of acetic acid with sodium hydroxide or sodium carbonate. This reaction forms sodium acetate and water. The compound can also be obtained from the reaction of sodium hydroxide with acetic anhydride.
Ionic precipitation reaction:2Na+(aq) + S2-(aq) + Pb2+(aq)+ 2(-OOCCH3)aq --> PbS2(s) + (2Na+(aq) + 2(-OOCCH3)aq)
water and salt........or sodium acetate and water.....or NaCH3COO + H2O
oxidation-reductionWhat type of a reaction occurs when a sodium hydroxide solution is mixed with an acetic acid solution?The answer above is wrong. The correct answer is acid-base neutralization
Commonly sodium chloride is not dissolved in organic compounds.
Glycine intracts with one mole of Bezoyl chloride in the presence of 10% (w/v) solution to yield hippuric acid with the elimination of one mole of hydrochloric acid. The excess of 10% NaOH solution serves two purposes, first; to remove unreacted benzoyl chloride. The NaOH solution hydrolyses the excess of benzoyl chloride present in reaction mixture, thereby resulting in formation of sodium chloride and sodium benzoate, which being water soluble remains in solution. Secondly the hydrochloric acid eliminated reacts with NaOH to yield NaCl. Both sodium benzoate and sodium chloride are water soluble, whereas the desired product hippuric acid being insoluble may be separated easily.