Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN: 9780618974122
Author: Andrei Straumanis
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 4, Problem 10E
Propanal (bp 48°C) and propanol (bp 97°C), both found on Table 4.2, have very similar surfaceareas and dipole moments. Construct an explanation for the large difference in boiling pointsbetween the two.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
19. Based on molecular mass and dipole moment of the five
compounds in the table below, which one should have the
highest boiling point?
Dipole Moment
(D)
Substance
Molecular Mass
(amu)
Propane, CH3CH2CH3
Dimethyl ether, CH3OCH3
Methylchloride, CH3C1
Acetaldehyde, CH;CHO
Acetonitrile, CH3CN
44
0.1
46
1.3
50
1.9
44
2.7
41
3.9
B) CH;CN
E) CH3CH2CH3
C) CH3CHO
A) CH3OCH3
D) CH;CI
Chapter 2
[References]
H3C
HB
CH3
На,
CH3
CH3
D
H3C
B
НО
Cholestanol differs from cholesterol only in the absence of a double bond in ring B.
Draw the three-dimensional structure of cholestanol, and then determine the orientation of the following groups:
#1: H at the junction of rings C & D with respect to ring C|
#2: H at the junction of rings A & B with respect to ring B
#3: Methyl at the junction of rings C & D with respect to ring C|
O I
a) Which of the following compounds is (are) capable of H-bonding to itself? Circle all that apply.
여
он
Но
но
A
в
D
E
b) Which of the compounds above cannot be a H-bond donor but can be a H-bond acceptor?
c) Which of the compounds above would you expect to have the highest boiling point?
Provide a brief explanation.
ZI
Chapter 4 Solutions
Organic Chemistry: A Guided Inquiry
Ch. 4 - Prob. 1CTQCh. 4 - Figure 4.1 is a cartoon depiction of liquid water...Ch. 4 - Prob. 3CTQCh. 4 - Prob. 4CTQCh. 4 - In HF , neither H nor F holds a full formal charge...Ch. 4 - Prob. 6CTQCh. 4 - Prob. 7CTQCh. 4 - Prob. 8CTQCh. 4 - Within any one section of Table 4.2, boiling...Ch. 4 - Prob. 10CTQ
Ch. 4 - Prob. 11CTQCh. 4 - Prob. 12CTQCh. 4 - Prob. 13CTQCh. 4 - Prob. 14CTQCh. 4 - Prob. 15CTQCh. 4 - Prob. 16CTQCh. 4 - Prob. 17CTQCh. 4 - Prob. 18CTQCh. 4 - Prob. 19CTQCh. 4 - Prob. 20CTQCh. 4 - Prob. 21CTQCh. 4 - Prob. 22CTQCh. 4 - (E) Label each of the following as strong acid,...Ch. 4 - Prob. 24CTQCh. 4 - Draw the structure of the conjugate base of water....Ch. 4 - Does Cl have a conjugate acid? If so, what is it?...Ch. 4 - Draw the conjugate base of CH4 (methane).Ch. 4 - For the previous four questions, label each...Ch. 4 - Prob. 29CTQCh. 4 - According to the conventions above, what is the...Ch. 4 - Draw an arrow on Figure 4.13 representing Hrxn4 ....Ch. 4 - Prob. 32CTQCh. 4 - Add a + or above each curved arrow in Figure 4.11...Ch. 4 - Prob. 34CTQCh. 4 - Prob. 35CTQCh. 4 - Prob. 36CTQCh. 4 - Prob. 37CTQCh. 4 - Prob. 38CTQCh. 4 - Prob. 39CTQCh. 4 - Prob. 40CTQCh. 4 - Prob. 41CTQCh. 4 - Prob. 42CTQCh. 4 - Prob. 43CTQCh. 4 - Prob. 44CTQCh. 4 - Prob. 45CTQCh. 4 - Prob. 46CTQCh. 4 - For NH3 (ammonia) and H2O (water)... a. Use curved...Ch. 4 - Prob. 48CTQCh. 4 - Prob. 49CTQCh. 4 - Prob. 50CTQCh. 4 - Prob. 51CTQCh. 4 - Prob. 52CTQCh. 4 - Prob. 53CTQCh. 4 - Prob. 1ECh. 4 - Prob. 2ECh. 4 - Prob. 3ECh. 4 - Prob. 4ECh. 4 - Prob. 5ECh. 4 - Prob. 6ECh. 4 - Prob. 7ECh. 4 - Prob. 8ECh. 4 - Propanal (bp 48°C) and propanol (bp 97°C), both...Ch. 4 - Rank the following molecules from lowest to...Ch. 4 - Prob. 12ECh. 4 - For each molecule below, draw the conjugate acid...Ch. 4 - For each structure you drew in the answer to the...Ch. 4 - Mark each of the following statements True or...Ch. 4 - Organic chemistry is a bit like cooking. Later in...Ch. 4 - Prob. 17ECh. 4 - Prob. 18ECh. 4 - Are endothermic reactions favorable or...Ch. 4 - Prob. 20ECh. 4 - Is bond formation endothermic or exothermic? Write...Ch. 4 - Summarize the relationship between pKa and acid...Ch. 4 - Summarize the relationship between pKa and base...Ch. 4 - Prob. 25ECh. 4 - Consider the following bases: a. For each base...Ch. 4 - Prob. 27ECh. 4 - The following are equivalent ways of asking about...Ch. 4 - Prob. 29E
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
- 1a. 1b. 1c.arrow_forwardNitromethane is an organic compound with the molecular Draw a complete Lewis structure for the conjugate acid of nitromethane that shows all bonds, unshared electron pairs, and minimized formal charges, where appropriate. formula CH, NO,. Draw a complete Lewis structure that shows all bonds, unshared electron pairs, and minimized formal charges, where appropriate. H H 1. H : 0 :arrow_forwardCompare columns I and II, and write A if the value in column lis greater than in II B if the value in column Il is greater than in I cif both values are equal D if the value in columnI cannot be compared with that in II Delocalization of Negative Charge Column I Column II NH Narrow_forward
- Statement 1: The boiling point of compound2 is lower because of the number of bondingregions present Statement 2: Moreover the increased no. of sigmabonds result to more difficult distortion resulting to a stronger attractive force within the atoms prensent Which is true? Statement 1, 2, both, or nonearrow_forwardHelp!! Phosgene, Cl2C=O, has a smaller dipole moment than formaldehyde, H2C=O, even though it contains electronegative chlorine atoms in place of hydrogen. Provide an explanation for this observation.arrow_forwardProvide the structure for Compound X in the reaction scheme below. Include all lone pairs and formal charges. 1.-78 °C X÷A· Y÷F LDA -78 °C 2. NH4Cl Compound X H Compound Zarrow_forward
- 5. Consider the H-bonds shown below. O---H- R- C-R 0–H-- FH---O' Assume that each H-bond is formed by two dipoles in a line, and approximate each dipole as a pair of point charges (q1, -q1, q2, -q2) separated by a distance r1=r2 with the centers of the dipoles at distance D apart. Then, the potential energy of the collinear arrangement of two dipoles is U=2µ1 H2/(4te,D³). Assuming that each H-bond has an energy of 1OKJ/mol, and that the charges q1 and q2 are equivalent, use the equation for the potential energy of a collinear arrangement of two dipoles to estimate the moment of the dipoles (µ1 = µ2) involved. Now, assuming that the charge separation distance in each dipole is 1 angstrom, estimate the magnitude of the partial charges responsible for the H-bond (report your answer in units of elementary charge, not coulombs).arrow_forward2. Account for the bond angle differences between (i) H-C-H (109.5°) in methane and H-S-H (90°); H-C-H (109.5°) and H-O-H (107.5°) in water The H-S-H has two lone pairs; The H-O-H has two lone pairs The H-S-H has no hybridization at p-orbitals; The H-O-H has two lone pairs The H-S-H has two lone pairs; The H-O-H has no hybridization at p-orbitals The H-S-H has no hybridization at p-orbitals; The H-O-H has no hybridization at p- orbitalsarrow_forward11:54 AM Mon May 1 < Bupropion (Wellbutrin) is a common antidepressant. Identify the most electronegative atom in the molecule from those indicated (I-IV). H3C. H3C | HIN= C II I CH3 ere or pull up for additional resources HU CH3 ||| H c= HIC CIH Н Question 31 of 35 IV CI H A) I B) II C) III D) IV 85% Submitarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Mass Spectrometry; Author: Professor Dave Explains;https://www.youtube.com/watch?v=hSirWciIvSg;License: Standard YouTube License, CC-BY