Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 1, Problem 1.67P
Interpretation Introduction
Interpretation:
Dimethyl sulfide contains a functional group that is not listed in Table 1-6. The functional group in Table 1-6 whose reactivity might resemble to the reactivity of dimethyl sulfide is to be determined.
Concept introduction:
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Dimethyl sulfide contains a functional group that is not listed in Table 1-6. Which functional group in Table 1-6 do youthink its reactivity might resemble?H3C-S-CH3Dimethyl sulfide
O REPRESENTATIONS OF ORGANIC MOLECULES
Identifying organic functional groups in simple structures
Name the functional group shown in each molecule below. The first answer has been filled in for you.
molecule
HIC C- CH3
CH3-
CH3
1
CH–NH=
CH3
CH3
I
CH3- -CHOIC-
O
CH3
0=C- CH₂ - CH₂
1
OH
functional group
alkyne
H H
For the molecule below, what is the molecular formula and is it a structural, condensed or line formula?
H
エー
H-C-
H
C
-C-C-O-H
|H
CH3 H
Chapter 1 Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
Ch. 1 - Prob. 1.1PCh. 1 - Prob. 1.2PCh. 1 - Prob. 1.3PCh. 1 - Prob. 1.4PCh. 1 - Prob. 1.5PCh. 1 - Prob. 1.6PCh. 1 - Prob. 1.7PCh. 1 - Prob. 1.8PCh. 1 - Prob. 1.9PCh. 1 - Prob. 1.10P
Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Prob. 1.13PCh. 1 - Prob. 1.14PCh. 1 - Prob. 1.15PCh. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Prob. 1.19PCh. 1 - Prob. 1.20PCh. 1 - Prob. 1.21PCh. 1 - Prob. 1.22PCh. 1 - Prob. 1.23PCh. 1 - Prob. 1.24PCh. 1 - Prob. 1.25PCh. 1 - Prob. 1.26PCh. 1 - Prob. 1.27PCh. 1 - Prob. 1.28PCh. 1 - Prob. 1.29PCh. 1 - Prob. 1.30PCh. 1 - Prob. 1.31PCh. 1 - Prob. 1.32PCh. 1 - Prob. 1.33PCh. 1 - Prob. 1.34PCh. 1 - Prob. 1.35PCh. 1 - Prob. 1.36PCh. 1 - Prob. 1.37PCh. 1 - Prob. 1.38PCh. 1 - Prob. 1.39PCh. 1 - Prob. 1.40PCh. 1 - Prob. 1.41PCh. 1 - Prob. 1.42PCh. 1 - Prob. 1.43PCh. 1 - Prob. 1.44PCh. 1 - Prob. 1.45PCh. 1 - Prob. 1.46PCh. 1 - Prob. 1.47PCh. 1 - Prob. 1.48PCh. 1 - Prob. 1.49PCh. 1 - Prob. 1.50PCh. 1 - Prob. 1.51PCh. 1 - Prob. 1.52PCh. 1 - Prob. 1.53PCh. 1 - Prob. 1.54PCh. 1 - Prob. 1.55PCh. 1 - Prob. 1.56PCh. 1 - Prob. 1.57PCh. 1 - Prob. 1.58PCh. 1 - Prob. 1.59PCh. 1 - Prob. 1.60PCh. 1 - Prob. 1.61PCh. 1 - Prob. 1.62PCh. 1 - Prob. 1.63PCh. 1 - Prob. 1.64PCh. 1 - Prob. 1.65PCh. 1 - Prob. 1.66PCh. 1 - Prob. 1.67PCh. 1 - Prob. 1.68PCh. 1 - Prob. 1.69PCh. 1 - Prob. 1.70PCh. 1 - Prob. 1.71PCh. 1 - Prob. 1.72PCh. 1 - Prob. 1.73PCh. 1 - Prob. 1.74PCh. 1 - Prob. 1.75PCh. 1 - Prob. 1.76PCh. 1 - Prob. 1.77PCh. 1 - Prob. 1.78PCh. 1 - Prob. 1.79PCh. 1 - Prob. 1.80PCh. 1 - Prob. 1.81PCh. 1 - Prob. 1.82PCh. 1 - Prob. 1.1YTCh. 1 - Prob. 1.2YTCh. 1 - Prob. 1.3YTCh. 1 - Prob. 1.4YTCh. 1 - Prob. 1.5YTCh. 1 - Prob. 1.6YTCh. 1 - Prob. 1.7YTCh. 1 - Prob. 1.8YTCh. 1 - Prob. 1.9YTCh. 1 - Prob. 1.10YTCh. 1 - Prob. 1.11YTCh. 1 - Prob. 1.12YTCh. 1 - Prob. 1.13YTCh. 1 - Prob. 1.14YTCh. 1 - Prob. 1.15YTCh. 1 - Prob. 1.16YTCh. 1 - Prob. 1.17YT
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
- please write the number that corresponds to the correct Lewis structure for the molecule shown in the box below. H H H-C-C-Ö-Ö-H_C-H-C-Ö-H H structures? :O: H C-H-C-O-HH-C-Ö-Ö-C-H || CH3CO₂H ܪܬܐܒܪܘܘܢ || H :O: | || H-C-C-O-H ||| IV H-C-C=Ö-Ö-H write the numbers of the following bond-line structures that represent identical V IVarrow_forwardA student states that this structural formula represents a hydrocarbon. H H-C-C-0-H H H Is this student correct? O Yes, a hydrocarbon is any compound that contains a carbon backbone. Yes, a hydrocarbon is any compound that contains hydrogen, carbon, and oxygen. No, a hydrocarbon is any compound that contains hydrogen and carbon.arrow_forwardExplain in 1 - 3 sentences explain what the difference is between ionic and covalent bonds.arrow_forward
- Please show me the electron structures for 1-5arrow_forwardQ-10. Vinegar (a) + Baking Soda (b) → Sodium Acetate + Carbon dioxide + Water. Write the molecular formula of 'a' and 'b'.arrow_forwardplease answer both name of highlighted side chain compound H C=0 CH, CH CH,- CH, CH, H-C=0 CH, CH, CH, CH, CH, HO -C- CH-C- OH CH, CH,- CH,- CH,- CH, CH, CH, CH,- CH,- CH – CH,– CH, Classify each of these chemical compounds: type of compound (check all that apply) compound molecular ionic HCO,H organic O inorganic hydrocarbon molecular ionic HI organic inorganic hydrocarbon molecular ionic BasO4 O organic inorganic O hydrocarbon ぎーー ゴーゴーぎー O O0 OO00 000 000arrow_forward
- 3-57 What is: (a) A single bond? (b) A double bond? (c) A triple bond?arrow_forward10-15 How many electrons are in the valence shell of each of the following atoms? Write a Lewis structure for an atom of each element. (Hint: Use the Periodic Table.) (a) Carbon(b) Oxygen (c) Nitrogen(d) Fluorinearrow_forward3-79 Answer true or false. (a) The letters VSEPR stand for valence-shell electron-pair repulsion. (b) In predicting bond angles about a central atom in a covalent molecule, the VSEPR model considers only shared electron pairs (electron pairs involved in forming covalent bonds). (c) The VSEPR model treats the two electron pairs of a double bond as one region of electron density and the three electron pairs of a triple bond as one region of electron density. (d) In carbon dioxide, OCO, carbon is surrounded by four pairs of electrons and the VSEPR model predicts 109.5° for the OCO bond angle. (e) For a central atom surrounded by three regions of electron density, the VSEPR model predicts bond angles of 120°. (f) The geometry about a carbon atom surrounded by three regions of electron density is described as trigonal planar. (g) For a central atom surrounded by four regions of electron density, the VSEPR model predicts bond angles of 360°/4 = 90°. (h) For the ammonia molecule, NH3, the VSEPR model predicts HNH bond angles of 109.5°. (i) For the ammonium ion, NH4, the VSEPR model predicts HNH bond angles of 109.5°. (j) The VSEPR model applies equally well to covalent compounds of carbon, nitrogen, and oxygen. (k) In water, HOH, the oxygen atom forms covalent bonds to two other atoms, and therefore, the VSEPR model predicts an HOH bond angle of 180°. (l) If you fail to consider unshared pairs of valence electrons when you use the VSEPR model, you will arrive at an incorrect prediction. (m) Given the assumptions of the VSEPR model, the only bond angles it predicts for compounds of carbon, nitrogen, and oxygen are 109.5°, 120°, and 180°.arrow_forward
- 3-109 Until several years ago, the two chlorofluorocarbons (CFCs) most widely used as heat transfer media in refrigeration systems were Freon-li (trichloro fluoromethane, CC13F) and Freon-12 (dichiorodi fluoromethane, CCl2F2). Draw a three-dimensional representation of each molecule and indicate the Direction of it.s polarity.arrow_forwardThe following model is a representation of citric acid, the key substance in the so-called citric acid cycle, by which food molecules are metabolized in the body. Only the connections between atoms are shown; multiple bonds are not indicated. Complete the structure by indicating the positions of multiple bonds and lone-pair electrons (gray = C, red = O, ivory = H).arrow_forward3-29 Answer true or false. (a) According to the Lewis model of bonding, atoms bond together in such a way that each atom participating in the bond acquires an outer-shell electron configuration matching that of the noble gas nearest to it in atomic number. (b) Atoms that lose electrons to achieve a filled valence shell become cations and form ionic bonds with anions. (c) Atoms that gain electrons to achieve filled valence shells become anions and form ionic bonds with cations. (d) Atoms that share electrons to achieve filled valence shells form covalent bonds. (e) Ionic bonds tend to form between elements on the left side of the Periodic Table, and covalent bonds tend to form between elements on the right side of the Periodic Table. (f) Ionic bonds tend to form between a metal and a nonmetal. (g) When two nonmetals combine, the bond between them is usually covalent. (h) Electronegativity is a measure of an atom’s at traction for the electrons it shares in a chemical bond with another atom. (j) Electronegativity generally increases with atomic number. (j) Electronegativity generally increases with atomic weight. (k) Electronegativity is a periodic property. (l) Fluorine, in the upper-right corner of the Periodic Table, is the most electronegative element; hydrogen, in the upper-left corner, is the least electronegative element. (m)Electronegativity depends on both the nuclear charge and the distance of the valence electrons from the nucleus. (n) Electronegativity generally increases from left to right across a period of the Periodic Table. (o) Electronegativity generally increases from top to bottom in a column of the Periodic Table.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning
Types of bonds; Author: Edspira;https://www.youtube.com/watch?v=Jj0V01Arebk;License: Standard YouTube License, CC-BY