ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<
9th Edition
ISBN: 9781337034623
Author: McMurry
Publisher: CENGAGE C
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 1.SE, Problem 56AP
Interpretation Introduction
Interpretation:
The structure of three different substances that contain a carbon-carbon double bond with the formula C4H8 is to be given and the difference between them is to be stated.
Concept introduction:
When large number of carbons and hydrogens combine more than one structure is possible. The carbons can all be in a row giving straight chain compounds or they can branch leading to branched chain or can form rings leading to cyclic compounds. The hydrogens can be attached to the carbons having in mind that carbon is tetravalent.
To determine:
The structure of three different substances that contain a carbon-carbon double bond with the formula C4H8 and to state the difference between them.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Are the two carbon atoms of C2H5Cl equivalent?
How would you describe the molecular geometry of C2H2F2, and what are its bond angles?
Consider cyclooctatetraene,C8H8, which has the octagonal structure shown belowWhat experiments or calculations could you perform to determinewhether cyclooctatetraene exhibits resonance?
Chapter 1 Solutions
ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<
Ch. 1.3 - Give the ground-state electron configuration for...Ch. 1.3 - How many electrons does each of the following...Ch. 1.4 - Prob. 3PCh. 1.4 - Convert the following representation of ethane,...Ch. 1.4 - What are likely formulas for the following...Ch. 1.4 - Prob. 6PCh. 1.4 - Prob. 7PCh. 1.7 - Draw a line-bond structure for propane, CH3CH2CH3....Ch. 1.7 - Convert the following molecular model of hexane, a...Ch. 1.8 - Draw a line-bond structure for propene, CH3CH=CH2....
Ch. 1.8 - Draw a line-bond structure for 1, 3-butadiene,...Ch. 1.8 - Following is a molecular model of aspirin...Ch. 1.9 - Draw a line-bond structure for propyne, CH3C≡CH....Ch. 1.10 - Prob. 14PCh. 1.12 - Prob. 15PCh. 1.12 - Prob. 16PCh. 1.12 - The following molecular model is a representation...Ch. 1.SE - Convert each of the following molecular models...Ch. 1.SE - The following model is a representation of citric...Ch. 1.SE - The following model is a representation of...Ch. 1.SE - The following model is a representation of...Ch. 1.SE - How many valence electrons does each of the...Ch. 1.SE - Give the ground-state electron configuration for...Ch. 1.SE - Prob. 24APCh. 1.SE - Prob. 25APCh. 1.SE - Draw an electron-dot structure for acetonitrile,...Ch. 1.SE - Draw a line-bond structure for vinyl chloride,...Ch. 1.SE - Fill in any nonbonding valence electrons that are...Ch. 1.SE - Convert the following line-bond structures into...Ch. 1.SE - Convert the following molecular formulas into...Ch. 1.SE - Prob. 31APCh. 1.SE - Oxaloacetic acid, an important intermediate in...Ch. 1.SE - Prob. 33APCh. 1.SE - Potassium methoxide, KOCH3, contains both covalent...Ch. 1.SE - What is the hybridization of each carbon atom in...Ch. 1.SE - Prob. 36APCh. 1.SE - Prob. 37APCh. 1.SE - What bond angles do you expect for each of the...Ch. 1.SE - Propose structures for molecules that meet the...Ch. 1.SE - What kind of hybridization do you expect for each...Ch. 1.SE - Pyridoxal phosphate, a close relative of vitamin...Ch. 1.SE - Prob. 42APCh. 1.SE - Prob. 43APCh. 1.SE - Quetiapine, marketed as Seroquel, is a heavily...Ch. 1.SE - Tell the number of hydrogens bonded to each carbon...Ch. 1.SE - Why do you suppose no one has ever been able to...Ch. 1.SE - Allene, H2C=C=CH2, is somewhat unusual in that it...Ch. 1.SE - Allene (see Problem 1-47) is structurally related...Ch. 1.SE - Complete the electron-dot structure of caffeine,...Ch. 1.SE - Most stable organic species have tetravalent...Ch. 1.SE - A carbanion is a species that contains a...Ch. 1.SE - Divalent carbon species called carbenes are...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - Prob. 56APCh. 1.SE - Among the most common over-the-counter drugs you...
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
- Draw a line-bond structure for propane, CH3CH2CH3. Predict the value of each bond angle, and indicate the overall shape of the molecule.arrow_forwardHow many valence electrons are there in a correctly drawn Lewis structure for formamide, HCONH2 ( You should also be able to draw the lewis structure for this. Hint, the C is in the center with an O ,N and 1 H attached. The other H atoms are attached to the N)arrow_forwardWhat are 2 different molecules with the molecular formula (C7H14O2)arrow_forward
- Draw the structure(s) of the carboxylic acids with the molecular formula C6H12O that have a four-carbon chain.arrow_forwardFormamide, HC(O)NH2, is prepared at high pressures from carbon monoxide and ammonia, and serves as an industrial solvent (the parentheses around the O indicate that it is bonded only to the carbon atom and that the carbon atom is also bonded to the H and the N atoms). Two resonance forms (one with formal charges) can be written for formamide. Write both resonance structures, and predict the bond angles about the carbon and nitrogen atoms for each resonance form. Are they the same? Describe how the experimental determination of the HNH bond angle could be used to indicate which resonance form is more important.arrow_forwardTwo compounds have the molecular formula N3H3. One of the compounds, triazene, contains an NN bond; the other compound, triaziridene, does not. (a) Write the correct Lewis structures for each compound. (b) Approximate the bond angle between the three nitrogen atoms in each compound.arrow_forward
- Cyanogen has the formula C2N2. Propose a bonding scheme that gives each atom the correct number of covalent bonds. (Hint: the two carbon atoms are in the center of a linear molecule.)arrow_forward2. Draw all the discrete structures that can be obtained for the compound with the formula C3H4Cl2.arrow_forwardDecide for which of the following compounds cis-trans isomerism is possible and draw the trans isomer for that compound, clearly showing the geometry about the double bond.arrow_forward
- Predict the hybridization, geometry, and bond angles for the carbon atoms in acetylene, C2H2.arrow_forwardTwo compounds have the same molecular formula C2H2Br2 one has a dipole moment the other does not both compounds react with bromine Br2 to produce the same compounds this reaction is a general accepted test for double bonds and each bromine atom of Br2 adds to a different atom of the double bond what is the identity of the original compounds dascribe the argument you usearrow_forwardHow many different structural isomers are there for octahedral molecules with the general formula AX2Y3 if A is the inner atom and there are no X-Y, X-X and Y-Y bonds?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning