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Determine if NaNH2 is a suitable reagent to deprotonate the following compound. Explain why. Determine if NaNH<sub>2</sub> is a suitable reagent to deprotonate the following compound. Explain why.

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Yes.
The conjugate base is resonance sta...

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Draw the conjugate base of CH3C ≡ \equiv CH.

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Rank the following compounds in decreasing order (most to least) of acidity. Rank the following compounds in decreasing order (most to least)  of acidity.   A)  III>II>IV>I B)  II>IV>III>II C)  IV>III>II>I D)  IV>II>III>I E)  III>IV>II>I


A) III>II>IV>I
B) II>IV>III>II
C) IV>III>II>I
D) IV>II>III>I
E) III>IV>II>I

F) All of the above
G) None of the above

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Which of the indicated protons is most acidic? Explain your choice. Which of the indicated protons is most acidic? Explain your choice.

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H-I is most acidic because the...

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Which of the following compounds is most acidic?


A) CH3OH
B) HCl
C) CH3SH
D) CH3NH2

E) A) and C)
F) B) and C)

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For the following reaction, identify the Lewis acid and the Lewis base. For the following reaction, identify the Lewis acid and the Lewis base.

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Draw the conjugate acid of CH3OCH3

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For the following acid-base reaction, predict which side the equilibrium is favored. For the following acid-base reaction, predict which side the equilibrium is favored.   A)  favor right side B)  favor left side C)  neither


A) favor right side
B) favor left side
C) neither

D) A) and B)
E) A) and C)

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Which of the following solvents can be used with NaNH2?


A) CH3CH2OH
B) CH3OH
C) H2O
D) Liquid NH3

E) B) and C)
F) A) and D)

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Which is the conjugate base in the following reaction? Which is the conjugate base in the following reaction?   A)  I B)  II C)  III D)  IV E)  Both I & III


A) I
B) II
C) III
D) IV
E) Both I & III

F) A) and B)
G) All of the above

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A Lewis acid is defined as _____.


A) a proton donor
B) an electron pair donor
C) a hydroxide donor
D) an electron pair acceptor

E) B) and D)
F) B) and C)

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For the following acid-base reaction, predict which side the equilibrium is favored. For the following acid-base reaction, predict which side the equilibrium is favored.   A)  favor right side B)  favor left side C)  neither


A) favor right side
B) favor left side
C) neither

D) A) and C)
E) B) and C)

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For the following reaction identify the acid and the base and predict the products. Draw the curved arrow mechanism for the formation of products and predict the direction of the equilibrium. For the following reaction identify the acid and the base and predict the products. Draw the curved arrow mechanism for the formation of products and predict the direction of the equilibrium.

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For the following reaction label the acid, base, conjugate acid and conjugate base. For the following reaction label the acid, base, conjugate acid and conjugate base.

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For the following acid-base reaction, predict which side the equilibrium is favored. For the following acid-base reaction, predict which side the equilibrium is favored.   A)  favor right side B)  favor left side C)  neither


A) favor right side
B) favor left side
C) neither

D) All of the above
E) B) and C)

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Determine if NaNH2 is a suitable reagent to deprotonate the following compound. Determine if NaNH<sub>2</sub> is a suitable reagent to deprotonate the following compound.   A)  Yes B)  No


A) Yes
B) No

C) A) and B)
D) undefined

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Determine if H2O is a suitable reagent to protonate the following compound. Determine if H<sub>2</sub>O is a suitable reagent to protonate the following compound.   A)  yes B)  no


A) yes
B) no

C) A) and B)
D) undefined

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Which of the following compounds is most acidic? Which of the following compounds is most acidic?   A)  I B)  II C)  III D)  IV


A) I
B) II
C) III
D) IV

E) A) and B)
F) C) and D)

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Which is the conjugate base in the following reaction? Which is the conjugate base in the following reaction?   A)  I B)  II C)  III D)  IV E)  Both II & III


A) I
B) II
C) III
D) IV
E) Both II & III

F) A) and E)
G) A) and B)

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Determine if H2O is a suitable reagent to protonate the following compound. Explain why. Determine if H<sub>2</sub>O is a suitable reagent to protonate the following compound. Explain why.

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Yes.
The conjugate base of wat...

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