Answer:
Nitrile, amide, carboxylic acid, phenyl (aka. arene)
**There are so many functional groups, so I may list some you don't know. There may also be some that I am not aware of. However, these are all the ones I can see.**
Explanation:
Nitrile: (bottom-left) N triple bonded to C
Amide: (middle) N single bonded to 3 carbons
Carboxylic Acid: (bottom-right) C-CO2H
Phenyl: (top-right) six carbon ring with alternating double bonds
Answer:
HCHO₂(aq) + Na⁺(aq) + OH⁻(aq) ⟶ Na⁺(aq) + CHO₂⁻(aq) + H₂O(ℓ)
Explanation:
An ionic equation uses the symbols (aq) [aqueous] to indicate molecules and ions that are soluble in water, (s) [solid] to indicate insoluble solids, and (ℓ) to indicate substances (usually water) in the liquid state.
In this reaction, aqueous sodium hydroxide reacts with aqueous formic acid to form sodium formate and water.
1. Molecular equation
HCHO₂(aq) + NaOH(aq) ⟶ NaCHO₂(aq) + H₂O(ℓ)
2. Ionic equation
Sodium hydroxide and sodium formate are soluble ionic compounds, so we write them as hydrated ions.
HCHO₂(aq) + Na⁺(aq) + OH⁻(aq) ⟶ Na⁺(aq) + CHO₂⁻(aq) + H₂O(ℓ)
D. Experiments provided new evidence about the atom, I think, sorry if I’m wrong