Concept explainers
(a)
Interpretation: The conformation which is present in higher concentration when
Concept introduction: The change in Gibbs free energy is represented by
If the
Answer to Problem 6.40P
The equatorial conformation is present in higher concentration in the given compound.
Explanation of Solution
Given
The value of
The equilibrium reaction of monosubstituted cyclohexane is shown below.
Figure 1
The value of
The equatorial conformation is present in higher concentration in the given compound.
(b)
Interpretation: The
Concept introduction: The change in Gibbs free energy is represented by
If the
Answer to Problem 6.40P
The
Explanation of Solution
The values of
The both given values are greater than
If the
Therefore, the
The
(c)
Interpretation: The
Concept introduction: The change in Gibbs free energy is represented by
If the
Answer to Problem 6.40P
The
Explanation of Solution
The values of
The equilibrium constant
Therefore, the
The
(d)
Interpretation: The
Concept introduction: The change in Gibbs free energy is represented by
If the
Answer to Problem 6.40P
The value of
Explanation of Solution
Given
The values of
The relationship between
As the value of
The value of
(e)
Interpretation: The explanation corresponding to the relation of size of
Concept introduction: The change in Gibbs free energy is represented by
If the
Answer to Problem 6.40P
The large size of
Explanation of Solution
The value
The large size of
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Chapter 6 Solutions
ORGANIC CHEMISTRY
- (a) Draw the four isomers of C₅H₁₀O that can be oxidizedto an aldehyde. (b) Draw the three isomers of C₅H₁₀O that canbe oxidized to a ketone. (c) Draw the isomers of C₅H₁₀O that cannot be easily oxidized to an aldehyde or ketone. (d) Name any isomer that is an alcohol.arrow_forwardDraw the skeletal (bond-line) structures of all isomers of C4H8O (including configurational isomers) that contain an alkene and an ether. There should be 5 structures.arrow_forwardCompounds A and B are isomers of the molecular formula C9H19Br. Both yield the same alkene C in an elimination reaction. Hydrogenation of C yields the product 2,3,3,4 tetramethyl pentane. What are the structures of A, B, and C?arrow_forward
- (1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amidearrow_forwardDraw and name the eight isomeric alcohols with formula C5H12O.arrow_forward[10] 10] Q1. Do the following conversions as directed. Write the complete reaction equation. (a) Benzaldehyde to Benzoic Acid. (b) Propanal to 1-propanal (c) Cyclohexanone to Cyclohexanol (d) Acetaldehyde to Ethyl alcohol (e) Acetone to Iso-propyl alcoholarrow_forward
- What is the relationship of these two structures?arrow_forwardQuestion: In an organic chemistry laboratory, a student is performing a reaction to synthesize a compound. The reaction involves the conversion of an alcohol into an alkene using a dehydration process. The student chooses to use concentrated sulfuric acid (H2SO4) as the catalyst for this reaction. However, during the reaction, the student notices that another product is formed along with the desired alkene. (a) What is the likely identity of the unexpected product formed during the reaction? Explain your answer. (b) Provide a plausible explanation for the formation of the unexpected product and suggest a modification to the reaction conditions that would favor the desired alkene as the major product.arrow_forwardFor cis-1,3-diethylcyciobutane, draw (a) a stereoisomer; (b) a constitutional isomer.arrow_forward
- Which of the following cycloalkanes are capable of geometric (cis-trans) isomerism?Draw the cis and trans isomers.(a) 3-ethyl-1,1-dimethylcyclohexane (b) 1-ethyl-3-methylcycloheptane(c) 1-ethyl-3-methylcyclopentane (d) 1-cyclopropyl-2-methylcyclohexanearrow_forward1. The structure of compound A is shown below. OH NH2 (a) Redraw the above structure in the form of expanded and condensed structures. (b) Determine the number of primary, secondary, tertiary and quaternary carbon atom that can be found in the compound. (c) Redraw, circle and name the functional groups present in the compound. (d) State the possible type of stereoisomerism of the compound and draw the appropriate structures to describe the isomerism.arrow_forwardDraw a chiral alkene with the formula C6H12.arrow_forward
- Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning