
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Question
Chapter 3.3B, Problem 3.6P
(a)
Interpretation Introduction
To determine: The structures and names corresponding to the five isomers of
Interpretation: The structures and names corresponding to the five isomers of
Concept introduction: The rules for the naming of
- Firstly the longest carbon chain is chosen and the naming of chain is done according to the number of carbon atoms that are present in the chain.
- Numbering of the chain is done in such a way that the substituent groups are placed at the lowest position.
- Naming of substituent groups is done by the replacing of –ane with –yl.
- If different types of substituent groups are present then they are written in an alphabetical order.
- If a substituent is present more than one time then prefixes like di, tri, tetra are used depending on the number of times that particular substituent group appears in the chain.
(b)
Interpretation Introduction
To determine: The structures and names corresponding to the nine isomers of
Interpretation: The structures and names corresponding to the nine isomers of
Concept introduction: The rules for the naming of alkanes are stated below.
- Firstly the longest carbon chain is chosen and the naming of chain is done according to the number of carbon atoms that are present in the chain.
- Numbering of the chain is done in such a way that the substituent groups are placed at the lowest position.
- Naming of substituent groups is done by the replacing of –ane with –yl.
- If different types of substituent groups are present then they are written in an alphabetical order.
- If a substituent is present more than one time then prefixes like di, tri, tetra are used depending on the number of times that particular substituent group appears in the chain.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Steps and explanation please
Steps and explanation please. Add how to solve or target similar problems.
Steps and explanation please. Add how to solve or target similar problems.
Chapter 3 Solutions
Organic Chemistry (9th Edition)
Ch. 3.2 - Using the general molecular formula for alkanes:...Ch. 3.3B - Name the following alkanes and haloalkanes. When...Ch. 3.3B - Write structures for the following compounds. a....Ch. 3.3B - Provide IUPAC names for the following compounds....Ch. 3.3B - Prob. 3.5PCh. 3.3B - Prob. 3.6PCh. 3.3B - Prob. 3.7PCh. 3.3B - Draw the structures of the following compounds. a....Ch. 3.3B - Without looking at the structures, give molecular...Ch. 3.4C - Prob. 3.10P
Ch. 3.7B - Prob. 3.11PCh. 3.7C - Draw a graph similar to Figure 3-9, of the...Ch. 3.8B - Draw a graph similar to Figure 3-11, of the...Ch. 3.9 - Draw a perspective representation of the most...Ch. 3.10C - Give IUPAC names for the following compounds.Ch. 3.10C - Draw the structure and give the molecular formula...Ch. 3.11 - Which of the following cycloalkanes are capable of...Ch. 3.11 - Give IUPAC names for the following cycloalkanes.Ch. 3.12B - The heat of combustion of...Ch. 3.12C - Prob. 3.20PCh. 3.13B - The cyclohexane chair shown in Figure 3-22 has the...Ch. 3.13B - Draw 1,2,3,4,5,6-hexamethylcyclohexane with all...Ch. 3.14 - Prob. 3.23PCh. 3.14 - Prob. 3.24PCh. 3.14 - Draw the most stable conformation of a....Ch. 3.15 - Prob. 3.26PCh. 3.15 - a. Draw both chair conformations of cis-1...Ch. 3.15 - Prob. 3.28PCh. 3.15A - Draw the two chair conformations of each of the...Ch. 3.15B - Draw the most stable conformation of a....Ch. 3.16A - Name the following compounds.Ch. 3.16B - Prob. 3.32PCh. 3 - Prob. 3.33SPCh. 3 - Prob. 3.34SPCh. 3 - 3-35 a. Draw and name the five cycloalkane...Ch. 3 - Draw the structure that corresponds with each...Ch. 3 - Each of the following descriptions applies to more...Ch. 3 - Write structures for a homologous series of...Ch. 3 - Prob. 3.39SPCh. 3 - Construct a graph, similar to Figure 3-11, of the...Ch. 3 - The following names are all incorrect or...Ch. 3 - In each pair of compounds, which compound has the...Ch. 3 - There are eight different five-carbon alkyl...Ch. 3 - Use a Newman projection about the indicated bond...Ch. 3 - a. Draw the two chair conformations of...Ch. 3 - Draw the two chair conformations of each compound,...Ch. 3 - Using what you know about the conformational...Ch. 3 - Prob. 3.48SPCh. 3 - Draw Newman projections along the C3C4 bond to...Ch. 3 - Prob. 3.50SPCh. 3 - The most stable form of the common sugar glucose...Ch. 3 - This is a Newman projection of a substituted...
Knowledge Booster
Similar questions
- Steps and explanation please. Add how to solve or target similar problems.arrow_forwardWould the following organic synthesis occur in one step? Add any missing products, required catalysts, inorganic reagents, and other important conditions. Please include a detailed explanation and drawings showing how the reaction may occur in one step.arrow_forwardThis organic molecule is dissolved in an acidic aqueous solution: OH OH A short time later sensitive infrared spectroscopy reveals the presence of a new C = O stretch absorption. That is, there must now be a new molecule present with at least one C = O bond. In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule. Videos 849 Explanation Check C Click and drag to start dwing a structure. # 3 MAR 23 Add/Remove steparrow_forward||| 7:47 ull 57% ← Problem 19 of 48 Submit Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the product of this carbocation rearrangement. Include all lone pairs and charges as appropriate. H 1,2-alkyl shift +arrow_forwardWould the following organic synthesis occur in one step? Add any missing products, required catalysts, inorganic reagents, and other important conditions. Please include a detailed explanation and drawings showing how the reaction may occur in one step.arrow_forwardBelow is the SN1 reaction of (S)-3-chlorocyclohexene and hydroxide (OH). Draw the missing curved arrows, lone pairs of electrons, and nonzero formal charges. In the third box, draw the two enantiomeric products that will be produced. 5th attempt Please draw all four bonds at chiral centers. Draw the two enantiomeric products that will be produced. Draw in any hydrogen at chiral centers. 1000 4th attempt Feedback Please draw all four bonds at chiral centers. 8. R5 HO: See Periodic Table See Hint H Cl Br Jid See Periodic Table See Hintarrow_forwardShow that a molecule with configuration π4 has a cylindrically symmetric electron distribution. Hint: Let the π orbitals be equal to xf and yf, where f is a function that depends only on the distance from the internuclear axis.arrow_forward(a) Verify that the lattice energies of the alkali metal iodides are inversely proportional to the distances between the ions in MI (M = alkali metal) by plotting the lattice energies given below against the internuclear distances dMI. Is the correlation good? Would a better fit be obtained by plotting the lattice energies as a function of (1 — d*/d)/d, as theoretically suggested, with d* = 34.5 pm? You must use a standard graphing program to plot the graph. It generates an equation for the line and calculates a correlation coefficient. (b) From the graph obtained in (a), estimate the lattice energy of silver iodide. (c) Compare the results of (b) with the experimental value of 886 kJ/mol. If they do not agree, explain the deviation.arrow_forwardCan I please get help with #3 & 4? Thanks you so much!arrow_forwardarrow_back_iosSEE MORE QUESTIONSarrow_forward_ios