Considering the two compounds shown below, which is more acidic and why? F y A OH VS. B OH A is the stronger acid because its conjugate base is better stabilized by resonance. OB is the stronger acid because its conjugate base is better stabilized by inductive effects. B is the stronger acid because its conjugate base is better stabilized by resonance. A is the stronger acid because its conjugate base is better stabilized by inductive effects.
Ionic Equilibrium
Chemical equilibrium and ionic equilibrium are two major concepts in chemistry. Ionic equilibrium deals with the equilibrium involved in an ionization process while chemical equilibrium deals with the equilibrium during a chemical change. Ionic equilibrium is established between the ions and unionized species in a system. Understanding the concept of ionic equilibrium is very important to answer the questions related to certain chemical reactions in chemistry.
Arrhenius Acid
Arrhenius acid act as a good electrolyte as it dissociates to its respective ions in the aqueous solutions. Keeping it similar to the general acid properties, Arrhenius acid also neutralizes bases and turns litmus paper into red.
Bronsted Lowry Base In Inorganic Chemistry
Bronsted-Lowry base in inorganic chemistry is any chemical substance that can accept a proton from the other chemical substance it is reacting with.
![**3.4 Brønsted-Lowry Acidity: Factors Affecting the Stability of Anions**
*Considering the two compounds shown below, which is more acidic and why?*
[Diagrams of two compounds]
- Compound A: Structure includes a fluorine atom (F), an alcohol group (OH), and a keto group (C=O).
- Compound B: Similar to A but with the positions of the fluorine and alcohol group switched.
**Options:**
- ○ A is the stronger acid because its conjugate base is better stabilized by resonance.
- ○ B is the stronger acid because its conjugate base is better stabilized by inductive effects.
- ○ B is the stronger acid because its conjugate base is better stabilized by resonance.
- ○ A is the stronger acid because its conjugate base is better stabilized by inductive effects.
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