ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
12th Edition
ISBN: 9781119304241
Author: Solomons
Publisher: WILEY C
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Textbook Question
Chapter 3, Problem 22P
What is the conjugate acid of each of the following bases?
(a)
(e)
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Concentration
Trial1
Concentration of iodide solution (mA)
255.8
Concentration of thiosulfate solution (mM)
47.0
Concentration of hydrogen peroxide solution (mM)
110.1
Temperature of iodide solution ('C)
25.0
Volume of iodide solution (1) used (mL)
10.0
Volume of thiosulfate solution (5:03) used (mL)
Volume of DI water used (mL)
Volume of hydrogen peroxide solution (H₂O₂) used (mL)
1.0
2.5
7.5
Time (s)
16.9
Dark blue
Observations
Initial concentration of iodide in reaction (mA)
Initial concentration of thiosulfate in reaction (mA)
Initial concentration of hydrogen peroxide in reaction (mA)
Initial Rate (mA's)
Draw the condensed or line-angle structure for an alkene with the formula C5H10.
Note: Avoid selecting cis-/trans- isomers in this exercise.
Draw two additional condensed or line-angle structures for alkenes with the formula C5H10.
Record the name of the isomers in Data Table 1.
Repeat steps for 2 cyclic isomers of C5H10
Explain why the following names of the structures are incorrect.
CH2CH3
CH3-C=CH-CH2-CH3
a. 2-ethyl-2-pentene
CH3
|
CH3-CH-CH2-CH=CH2
b. 2-methyl-4-pentene
Chapter 3 Solutions
ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
Ch. 3 - Prob. 1PPCh. 3 - PRACTICE PROBLEM 3.2
Write equations showing the...Ch. 3 - PRACTICE PROBLEM 3.3 Which of the following are...Ch. 3 - Prob. 4PPCh. 3 - PRACTICE PROBLEM 3.5 Formic acid (HCO2H) has...Ch. 3 - Prob. 6PPCh. 3 - Prob. 7PPCh. 3 - Prob. 8PPCh. 3 - PRACTICE PROBLEM 3.9 Predict the outcome of the...Ch. 3 - Prob. 10PP
Ch. 3 - Prob. 11PPCh. 3 - Prob. 12PPCh. 3 - Prob. 13PPCh. 3 - Prob. 14PPCh. 3 - PRACTICE PROBLEM 3.15 Nitro groups have a large...Ch. 3 - PRACTICE PROBLEM 3.16
Your laboratory instructor...Ch. 3 - Prob. 17PPCh. 3 - Prob. 18PPCh. 3 - Prob. 19PPCh. 3 - What is the conjugate base of each of the...Ch. 3 - List the bases you gave as answers to Problem 3.20...Ch. 3 - 3.22 What is the conjugate acid of each of the...Ch. 3 - List the acids you gave as answers to Problem 3.22...Ch. 3 - Rank the following in order of increasing acidity.Ch. 3 - Without consulting tables, select the stronger...Ch. 3 - Designate the Lewis acid and Lewis base in each of...Ch. 3 - Prob. 27PCh. 3 - Prob. 28PCh. 3 - Write an equation, using the curved-arrow...Ch. 3 - 3.30 What reaction will take place if ethyl...Ch. 3 - 3.31 (a) The of formic acid. What is the? (b)...Ch. 3 - Acid HA has pKa=20; acid HB has pKa=10. (a) Which...Ch. 3 - Prob. 33PCh. 3 - 3.34 (a) Arrange the following compounds in order...Ch. 3 - 3.35 Arrange the following compounds in order of...Ch. 3 - 3.36 Arrange the following in order of increasing...Ch. 3 - Prob. 37PCh. 3 - 3.38 Supply the curved arrows necessary for the...Ch. 3 - Glycine is an amino acid that can be obtained from...Ch. 3 - 3.40 Malonic acid, , is a diprotic acid. The for...Ch. 3 - 3.41 The free-energy change, , for the ionization...Ch. 3 - 3.42 At the enthalpy change, , for the ionization...Ch. 3 - The compound at right has (for obvious reasons)...Ch. 3 - 3.44.
(a) Given the above sequence of...Ch. 3 - Prob. 45PCh. 3 - Prob. 46PCh. 3 - 3.47 As noted in Table 3.1, the of acetone, , is...Ch. 3 - Formamide (HCONH2) has a pKa of approximately 25....Ch. 3 - List all the chemical species likely to be present...Ch. 3 - Prob. 2LGPCh. 3 - Prob. 3LGPCh. 3 - Prob. 4LGP
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