Concept explainers
(a)
Interpretation:
The
(a)

Explanation of Solution
The equilibrium reaction is given below.
The acid ionization constant can be written as given below.
A table can be set up as shown below.
The concentration of
At equilibrium,
Then,
The
Therefore, the
(b)
Interpretation:
The
(b)

Explanation of Solution
The equilibrium reaction is given below.
The acid ionization constant can be written as given below.
A table can be set up as shown below.
The concentration of
At equilibrium,
Assuming x is very small, it can be written
Then,
The
Therefore, the
(c)
Interpretation:
The
(c)

Explanation of Solution
The equilibrium reaction is given below.
The base ionization constant can be written as given below.
A table can be set up as shown below.
The concentration of
At equilibrium,
Assuming x is very small, it can be written
Then,
The
Therefore, the
(d)
Interpretation:
The
(d)

Explanation of Solution
The concentration of
The equilibrium reaction is given below.
The base ionization constant can be written as given below.
A table can be set up as shown below.
The concentration of
At equilibrium,
Assuming x is very small, it can be written
Then,
The
Therefore, the
(e)
Interpretation:
The
(e)

Explanation of Solution
The reaction of
The concentration of
The
Therefore, the
(f)
Interpretation:
The
(f)

Explanation of Solution
A table can be set up as shown below.
The concentration of
At equilibrium,
Then,
The
Therefore, the
(g)
Interpretation:
The
(g)

Explanation of Solution
A table can be set up as shown below.
The concentration of
At equilibrium,
Then,
Assuming x is very small, it can be written
The
Therefore, the
(h)
Interpretation:
The
(h)

Explanation of Solution
Neither of these ions affect the
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Chapter 14 Solutions
OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
- Imagine each of the molecules shown below was found in an aqueous solution. Can you tell whether the solution is acidic, basic, or neutral? molecule 0=0 H3N-CH-C-o HO CH2 OH The solution is... O acidic O basic O neutral O (unknown) H₂N acidic O basic O neutral ○ (unknown) + H3N O OH O acidic O basic O neutral O (unknown) H2N-CH-C-O CH3 O acidic O basic neutral ○ (unknown) X ? olo HEarrow_forwardRecognizing ampli Draw an a amino acid with a methyl (-CH3) side chain. Explanation Check Click and drag to start drawing a structure. X Carrow_forwardWrite the systematic name of each organic molecule: structure name × HO OH ☐ OH CI CI O CI OH OHarrow_forward
- く Check the box under each a amino acid. If there are no a amino acids at all, check the "none of them" box under the table. Note for advanced students: don't assume every amino acid shown must be found in nature. COO H3N-C-H CH2 HO CH3 NH3 O CH3-CH CH2 OH Onone of them Explanation Check + H3N O 0. O OH + NH3 CH2 CH3-CH H2N C-COOH H O HIC + C=O H3N-C-O CH3- - CH CH2 OH Х 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Accesarrow_forwardWrite the systematic name of each organic molecule: structure HO-C-CH2-CH3 O -OH CH3-CH2-CH2-CH2-CH2-C-OH CH3 CH3-CH-CH2-C-OH Explanation Check S namearrow_forwardtheres 2 productsarrow_forward
- Draw the major product of this solvolysis reaction. Ignore any inorganic byproducts. + CH3CH2OH Drawing Q Atoms, Bonds and Rings OCH2CH3 || OEt Charges OH 00-> | Undo Reset | Br Remove Done Drag To Pan +arrow_forwardDraw the major product of this SN1 reaction. Ignore any inorganic byproducts. CH3CO2Na CH3CO2H Drawing + Br Q Atoms, Bonds and Rings OAC Charges OH ОАс Na ဂ Br Undo Reset Remove Done Drag To Pan +arrow_forwardOrganic Functional Groups entifying positions labeled with Greek letters in acids and derivatives 1/5 ssible, replace an H atom on the a carbon of the molecule in the drawing area with a ce an H atom on the ẞ carbon with a hydroxyl group substituent. ne of the substituents can't be added for any reason, just don't add it. If neither substi er the drawing area. O H OH Oneither substituent can be added. Check D 1 Accessibility ado na witharrow_forward
- Differentiate between electrophilic and nucleophilic groups. Give examples.arrow_forwardAn aldehyde/ketone plus an alcohol gives a hemiacetal, and an excess of alcohol gives an acetal. The reaction is an equilibrium; in aldehydes, it's shifted to the right and in ketones, to the left. Explain.arrow_forwardDraw a Haworth projection or a common cyclic form of this monosaccharide: H- -OH H- OH H- -OH CH₂OHarrow_forward
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