Organic Chemistry Acidity and Reactions

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Questions and Answers

Rank the indicated protons in terms of most acidic to least acidic from the following options.

  • Most acidic: Induction, Middle: Resonance, Least acidic: Atom
  • Most acidic: Resonance, Middle: Atom, Least acidic: Induction (correct)
  • Most acidic: Induction, Middle: Atom, Least acidic: Resonance
  • Most acidic: Atom, Middle: Induction, Least acidic: Resonance

Which of the following statements accurately explains the ranking of OH vs. NH in terms of acidity?

  • O is less electronegative than N, making OH weaker.
  • The atom effect indicates that O more electronegative makes OH stronger. (correct)
  • Resonance effect favors NH over OH.
  • The charge effect favors NH over OH based on electron distribution.

In a Bronsted-Lowry acid-base reaction, what do you look for when predicting the products?

  • The presence of inert gases
  • Temperature effects on reactant states
  • The concentration of reactants only
  • The strength of the acids and bases involved (correct)

What is the IUPAC name for 4-ethyl-2-methylhexane?

<p>2,4-dimethylhexane (B)</p> Signup and view all the answers

Which factor has lesser importance in determining the strength of acidity among these options?

<p>Orbital effect (D)</p> Signup and view all the answers

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Study Notes

Ranking Acidity

  • CARIO effects help determine acidity:
    • Atom: More electronegative atoms make an acid stronger.
    • Resonance: More resonance stabilization of the conjugate base makes an acid stronger.
    • Induction: Electron-withdrawing groups increase acidity by stabilizing the conjugate base.
    • Charge: A more positive charge makes an acid stronger.
    • Orbital: Hybridization affects acidity. sp orbitals are more acidic than sp2, which are more acidic than sp3.

Acid-Base Reactions

  • Brønsted-Lowry acid-base reactions involve the transfer of a proton (H+).
    • Stronger acids donate protons more readily.
    • Weaker acids hold onto protons more tightly.

Organic Molecules

  • Nomenclature follows IUPAC rules:
    • Parent chain: The longest continuous carbon chain.
    • Substituents: Groups attached to the parent chain.
    • Numbers: Locate substituents on the parent chain.

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