Zwitterion is an ion consists of equal positive and negative charges on the same molecule which make it more stable and has high melting point
p-aminobenzene sulfonic acid contains both acidic (-SO₃H) and basic groups (NH₂), the acidic group will lose one proton to give (-SO₃⁻) and the basic group will gain this proton to give (-NH₃⁺)
The structure is:
For this question, I think it is the other way around. It is true that chloroacetic acid is stronger in strength than acetic acid. Acid strength is measured as the equilibrium constant of the reaction <span>HA -----> H+ + A-
</span><span> In acetic acid, the anion produced by dissociation is CH3-COO-; in chloroacetic acid it is CH2Cl-COO-. Comparing the two, in the first one the negative charge is taken up mostly by the two oxygen atoms. In the second there is also an electronegative chlorine atom nearby to draw more charge towards itself. Therefore, the charge is less concentrated in the chloroacetate ion than it is in the acetate ion, and, accordingly, chloroacetic acid is stronger than acetic acid. </span>
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May the gods ever be in your favor.
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What's Dis Suppose To Mean ?
So I’m not 100% sure what you’re asking but I’m going to give it a go. The elimination reaction is a term used in organic chemistry that describes a type of reactions. The name kinda tells you what’s going to happen. Something is going to be removed/eliminated from initial reactant/substrate and as a result, an alkene (double bond containing compound) will form.
In elimination reactions a hydrogen atom is first removed (as a H+) from the beta carbon. As a result, the left behind electrons create a pi bond between the beta carbon and the neighboring alpha carbon. This promotes the electronegative atom, on the alpha carbon, to leaves the substrate taking both electrons from the shared sigma bond with the alpha carbon.