12. While each molecule below has more protons (H-atoms) than being shown, just focus on the protons identified. Compare the two protons identified. 1) Draw the two conjugate bases that could possibly result (althou gh one will be preferred over the other). The purpose here is to make you look at the conjugate base and the atom upon which the negative charge resides, then you should consider your SERIO factors. 2) Identify which proton is more acidic by circling the H, or H, on the original molecule. 3) Explain why by comparing the conjugate bases. Cirele the factor you considered when comparing the stabilities of the conjugate bases. Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization СвА св, Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization св, св, Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization O-He CBA св, Explanation Size Electronegativity Resonance Inductive effect Orbital hybridization св, св, Explanation Size Electronegativity Resonance Inductive effect Orbital hybridization он, Н,о свА св, Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization св, св,

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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12. While each molecule below has more protons (H-atoms) than being shown, just focus on the protons identified.
Compare the two protons identified.
1) Draw the two conjugate bases that could possibly result (althou gh one will be preferred over the other). The
purpose here is to make you look at the conjugate base and the atom upon which the negative charge resides,
then you should consider your SERIO factors.
2) Identify which proton is more acidic by circling the H, or H, on the original molecule.
3) Explain why by comparing the conjugate bases. Cirele the factor you considered when comparing the
stabilities of the conjugate bases.
Explanation:
Size
Electronegativity
Resonance
Inductive effect
Orbital hybridization
СвА
св,
Explanation:
Size
Electronegativity
Resonance
Inductive effect
Orbital hybridization
св,
св,
Transcribed Image Text:12. While each molecule below has more protons (H-atoms) than being shown, just focus on the protons identified. Compare the two protons identified. 1) Draw the two conjugate bases that could possibly result (althou gh one will be preferred over the other). The purpose here is to make you look at the conjugate base and the atom upon which the negative charge resides, then you should consider your SERIO factors. 2) Identify which proton is more acidic by circling the H, or H, on the original molecule. 3) Explain why by comparing the conjugate bases. Cirele the factor you considered when comparing the stabilities of the conjugate bases. Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization СвА св, Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization св, св,
Explanation:
Size
Electronegativity
Resonance
Inductive effect
Orbital hybridization
O-He
CBA
св,
Explanation
Size
Electronegativity
Resonance
Inductive effect
Orbital hybridization
св,
св,
Explanation
Size
Electronegativity
Resonance
Inductive effect
Orbital hybridization
он,
Н,о
свА
св,
Explanation:
Size
Electronegativity
Resonance
Inductive effect
Orbital hybridization
св,
св,
Transcribed Image Text:Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization O-He CBA св, Explanation Size Electronegativity Resonance Inductive effect Orbital hybridization св, св, Explanation Size Electronegativity Resonance Inductive effect Orbital hybridization он, Н,о свА св, Explanation: Size Electronegativity Resonance Inductive effect Orbital hybridization св, св,
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