For conjugate acid–base pairs, how are K a and K b related? Consider the reaction of acetic acid in water CH 3 CO 2 H ( a q ) + H 2 O ( l ) ⇌ CH 3 CO 2 − ( a q ) + H 3 O + ( a q ) where K a = 1.8 × 10 −5 a. Which two bases are competing for the proton? b. Which is the stronger base? c. In light of your answer to part b. why do we classify the acetate ion (CH 3 CO 2 − ) as a weak base? Use an appropriate reaction to justify your answer. In general, as base strength increases, conjugate acid strength decreases. Explain why the conjugate acid of the weak base NH 3 is a weak acid. To summarize, the conjugate base of a weak acid is a weak base and the conjugate acid of a weak base is a weak acid (weak gives you weak). Assuming K a for a monoprotic strong acid is 1 × 10 6 , calculate K b for the conjugate base of this strong acid. Why do conjugate bases of strong acids have no basic properties in water? List the conjugate bases of the six common strong acids. To tie it all together, some instructors have students think of Li + , K + , Rb + , Cs + , Ca 2+ , Sr 2+ , and Ba 2+ as the conjugate acids of the strong bases LiOH, KOH. RbOH, CsOH, Ca(OH) 2 , Sr(OH) 2 , and Ba(OH) 2 . Although not technically correct, the conjugate acid strength of these cations is similar to the conjugate base strength of the strong acids. That is, these cations have no acidic properties in water; similarly, the conjugate bases of strong acids have no basic properties (strong gives you worthless). Fill in the blanks with the correct response. The conjugate base of a weak acid is a_____base. The conjugate acid of a weak base is a_____acid. The conjugate base of a strong acid is a_____base. The conjugate acid of a strong base is a_____ acid. ( Hint: Weak gives you weak and strong gives you worthless.)
For conjugate acid–base pairs, how are K a and K b related? Consider the reaction of acetic acid in water CH 3 CO 2 H ( a q ) + H 2 O ( l ) ⇌ CH 3 CO 2 − ( a q ) + H 3 O + ( a q ) where K a = 1.8 × 10 −5 a. Which two bases are competing for the proton? b. Which is the stronger base? c. In light of your answer to part b. why do we classify the acetate ion (CH 3 CO 2 − ) as a weak base? Use an appropriate reaction to justify your answer. In general, as base strength increases, conjugate acid strength decreases. Explain why the conjugate acid of the weak base NH 3 is a weak acid. To summarize, the conjugate base of a weak acid is a weak base and the conjugate acid of a weak base is a weak acid (weak gives you weak). Assuming K a for a monoprotic strong acid is 1 × 10 6 , calculate K b for the conjugate base of this strong acid. Why do conjugate bases of strong acids have no basic properties in water? List the conjugate bases of the six common strong acids. To tie it all together, some instructors have students think of Li + , K + , Rb + , Cs + , Ca 2+ , Sr 2+ , and Ba 2+ as the conjugate acids of the strong bases LiOH, KOH. RbOH, CsOH, Ca(OH) 2 , Sr(OH) 2 , and Ba(OH) 2 . Although not technically correct, the conjugate acid strength of these cations is similar to the conjugate base strength of the strong acids. That is, these cations have no acidic properties in water; similarly, the conjugate bases of strong acids have no basic properties (strong gives you worthless). Fill in the blanks with the correct response. The conjugate base of a weak acid is a_____base. The conjugate acid of a weak base is a_____acid. The conjugate base of a strong acid is a_____base. The conjugate acid of a strong base is a_____ acid. ( Hint: Weak gives you weak and strong gives you worthless.)
Solution Summary: The author explains the relationship between the conjugate base of a weak acid and the base dissociation constant.
For conjugate acid–base pairs, how are Ka and Kb related? Consider the reaction of acetic acid in water
CH
3
CO
2
H
(
a
q
)
+
H
2
O
(
l
)
⇌
CH
3
CO
2
−
(
a
q
)
+
H
3
O
+
(
a
q
)
where Ka = 1.8 × 10−5
a. Which two bases are competing for the proton?
b. Which is the stronger base?
c. In light of your answer to part b. why do we classify the acetate ion (CH3CO2−) as a weak base? Use an appropriate reaction to justify your answer.
In general, as base strength increases, conjugate acid strength decreases. Explain why the conjugate acid of the weak base NH3 is a weak acid.
To summarize, the conjugate base of a weak acid is a weak base and the conjugate acid of a weak base is a weak acid (weak gives you weak). Assuming Ka for a monoprotic strong acid is 1 × 106, calculate Kb for the conjugate base of this strong acid. Why do conjugate bases of strong acids have no basic properties in water? List the conjugate bases of the six common strong acids. To tie it all together, some instructors have students think of Li+, K+, Rb+, Cs+, Ca2+, Sr2+, and Ba2+ as the conjugate acids of the strong bases LiOH, KOH. RbOH, CsOH, Ca(OH)2, Sr(OH)2, and Ba(OH)2. Although not technically correct, the conjugate acid strength of these cations is similar to the conjugate base strength of the strong acids. That is, these cations have no acidic properties in water; similarly, the conjugate bases of strong acids have no basic properties (strong gives you worthless). Fill in the blanks with the correct response. The conjugate base of a weak acid is a_____base. The conjugate acid of a weak base is a_____acid. The conjugate base of a strong acid is a_____base. The conjugate acid of a strong base is a_____ acid. (Hint: Weak gives you weak and strong gives you worthless.)
Hi!!
Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required.
Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!
Hi!!
Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required.
Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!
. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the
molecule depicted below.
Bond B
2°C. +2°C. < cleavage
Bond A
• CH3 + 26. t cleavage
2°C• +3°C•
Bond C
Cleavage
CH3 ZC
'2°C. 26.
E
Strongest
3°C. 2C.
Gund
Largest
BDE
weakest bond
In that molecule
a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in
appropriate boxes.
Weakest
C bond
Produces
A
Weakest
Bond
Most
Strongest
Bond
Stable radical
Strongest Gund
produces least stable
radicals
b. (4pts) Consider the relative stability of all cleavage products that form when bonds A,
B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B,
and C are all carbon radicals.
i. Which ONE cleavage product is the most stable? A condensed or bond line
representation is fine.
人
8°C. formed in
bound C
cleavage
ii. Which ONE cleavage product is the least stable? A condensed or bond line
representation is fine.
methyl radical
•CH3
formed in
bund A Cleavage
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