EBK ESSENTIAL ORGANIC CHEMISTRY
3rd Edition
ISBN: 8220100659461
Author: Bruice
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Textbook Question
Chapter 13, Problem 27P
Explain why the pKa of a hydrogen bonded to the sp3 carbon of propene is greater (pKa = 42) than that of any of the carbon acids listed in Table 13.1, but is less than the pKa of an
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
2. Draw structures for the following systems. If more than one isomer is possible, draw strcutures
for all the possible isomers.
Benzene ring with
a methyl group
and a nitro group
(Draw all possible
isomers, and name
them)
Benzene ring
connected to a
heptane chain
(Draw all possible
isomers, and name
them)
2-benzyl-3-
methylbutan-1-ol
What accounts for the geometry (pyramidalization) of the NH2 group in aniline?
1. Resonance between the NH2 group and the benzene ring.
2. The electronic withdrawing nature of the sp2 carbons in the phenyl group.
3. Participation of the nitrogen lone pair to make the system aromatic.
4. Both 1 and 3.
True or False
1. With alkynes having 2 pi bonds, they have more electron-rich region than alkenes and, thus, are more reactive than alkenes.
2. Hydrobromination of an alkene follows anti-Markovnikov’s rule in the presence of a peroxide.
3. The reaction of BH3 with 2-methylbut-2-ene results in the attachment of a hydroxyl group, OH, on the third carbon since this carbon is less substituted.
4. The reduction of an alkyne using a strong base such as LiNH2 gives an alkane when 2 equivalents of hydrogen gas is added.
Chapter 13 Solutions
EBK ESSENTIAL ORGANIC CHEMISTRY
Ch. 13.1 - Identify the most acidic hydrogen in each...Ch. 13.1 - Prob. 2PCh. 13.1 - Prob. 3PCh. 13.1 - Prob. 4PCh. 13.1 - Explain why HO cannot remove a proton from the...Ch. 13.2 - Prob. 6PCh. 13.2 - Prob. 7PCh. 13.3 - Prob. 8PCh. 13.3 - Prob. 9PCh. 13.3 - Prob. 10P
Ch. 13.4 - Prob. 11PCh. 13.5 - Prob. 12PCh. 13.5 - Prob. 13PCh. 13.6 - Prob. 14PCh. 13.7 - Prob. 16PCh. 13.8 - Prob. 17PCh. 13.8 - Prob. 18PCh. 13.8 - Prob. 19PCh. 13.9 - Prob. 20PCh. 13.10 - Propose a mechanism for the formation of...Ch. 13.10 - Prob. 22PCh. 13.10 - a. If the biosynthesis of palmitic acid were...Ch. 13 - Draw the enol tautomers for each of the following...Ch. 13 - Number the following compounds in order from...Ch. 13 - Prob. 26PCh. 13 - Explain why the pKa of a hydrogen bonded to the...Ch. 13 - Prob. 28PCh. 13 - Prob. 29PCh. 13 - Prob. 30PCh. 13 - Prob. 31PCh. 13 - Prob. 32PCh. 13 - Prob. 33PCh. 13 - Using cyclopentanone as the reactant, show the...Ch. 13 - Prob. 35PCh. 13 - Prob. 36PCh. 13 - Prob. 37PCh. 13 - Prob. 38PCh. 13 - Prob. 39PCh. 13 - Prob. 40PCh. 13 - Prob. 41PCh. 13 - Prob. 42PCh. 13 - Prob. 43PCh. 13 - Prob. 44PCh. 13 - Describe how the following compounds can be...Ch. 13 - Prob. 46PCh. 13 - Which would require a higher temperature:...Ch. 13 - Prob. 48PCh. 13 - Propose a mechanism for the following reaction:Ch. 13 - Show how the following compounds could be...Ch. 13 - Prob. 51PCh. 13 - Prob. 52P
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- what is the role of conc. H2SO4 in molisch's reagent test?arrow_forwardGive a brief answer to explain why acetic acid has a much higher BP (118 C) than 1- propanol (BP = 97 C) even though they both have the same size (molecular weight = 60) and they both form Hydrogen bonds.arrow_forwardGive the organic reaction products for the following reaction a. b. a. b. CH3CH2-C. ง ว NaOH ? + ? N(CH3)2 H₂O H*/H₂O CH3-C-OCH2CH3 ? + ?arrow_forward
- Hh.148.arrow_forwardModified True or False. Write correct if the statement is True and if false write the word/s that make it false and beside it write the word/s that will make the statement true. 4. Lone pair delocalization decreases the positivity of carbonyl carbon.5. The longer the carbon chain, the higher the boiling point.6. sp3 is 75% p character and this allows C-H hyper conjugation.7. The higher the electronegativity, the higher the temperature needed to break bonds.8. Steric effect increases the boiling point.9. Stearic effect increases the Van der Waals forces.10. Lone pair delocalization decreases the positivity of carbonyl carbon.11. Amines are considered basic.12. The stronger the Van der Waals forces between molecules of the same substance, themore soluble the substance is in water.13. The longer the carbon chain, the lower the solubility of the substance in water.14. Alkanes with less than 6 carbon atoms are gases.15. Stearic effects enhances the solubility in water.16. H-bond can exist…arrow_forwardEarly structural studies on benzene had to explain the following experimental evidence. When benzene was treated with Br2 (plus a Lewis acid), a single substitution product of molecular formula C6H5Br was formed. When this product was treated with another equivalent of Br2, three different compounds of molecular formula C6H4Br2 were formed.a. Explain why a single Kekulé structure is consistent with the first result, but does not explain the second result.b. Then explain why a resonance description of benzene is consistent with the results of both reactions.arrow_forward
- This question is correct but can someone explain to me how I can tell the difference on these examples between hemiactal and acetal? Thank you so much! ☺arrow_forwardTo which class of alcohols (1°, 2° or 3°) do each of the possible products (A/B) belong?arrow_forwardAccount for the fact that treating propenoic acid (acrylic acid) with HCl gives only 3-chloropropanoic acid.arrow_forward
- 4. A hydrocarbon with IHD of 2 showed a persisting yellow color in the bromine test. What is the likely identity of the compound? a bicyclic compound an alkene a benzene ring an alkyne a straight chain hydrocarbonarrow_forwardWhich of the following area. hemiacetals? b. acetals? c. hydrates?arrow_forward5. Which is the correct assignment of the names of the following substituted benzenes? CH3 OH &&0 OH OH = 1 2 a. 1 phenol; 2 = m-cresol; 3= toluene = b. 1 = m-cresol; 2 = resorcinol; 3= m-xylene c. 1 = anisole; 2 = catechol; 3 = m-xylene d. 1 3 m-cresol; 2 anisole; 3 = cumene CH3arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Seven Name Reactions in One - Palladium Catalysed Reaction (047 - 053); Author: Rasayan Academy - Jagriti Sharma;https://www.youtube.com/watch?v=5HEKTpDFkqI;License: Standard YouTube License, CC-BY