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
Want to see more full solutions like this?
Chapter 6 Solutions
PKG ORGANIC CHEMISTRY
- Question: 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_forwardName the family to which each organic compound belongs. The first answer has been filled in for you. compound CH₂ || CH₂-C-0-C- CH₂ O || CH₂ || CH–C—NH, CH, OH I | CH₂-CH-C || || CH,—C–NH CH, X family ester 0arrow_forward1,1-dichloropropane reacts with aqueous sodium hydroxide in a series of steps to give propanal. NAOH(aq) CH,CH,CHCI, CH,CH,CHO Which term describes the first step of this reaction? A addition B elimination C oxidation D substitutionarrow_forward
- Draw the structure and name the product formed if the following alcohols are oxidized. Assume that an excess of oxidising agent is used.(i) CH3CH2CH2CH2OH(ii) 2-butanol(iii) 2-methyl-l-propanolarrow_forwardPyrethrins, such as jasmolin II (shown below), are a group of natural compounds that are synthesized by flowers of the genus Chrysanthemum (known as pyrethrum flowers) to act as insecticides. CH3 CH2=CH-CH. CH-C- -HCS 0-CH, CH,-C H2C- ČH, Which is not a functional group or structural feature in jasmolin II? cycloalkane carboxylic acid ester alkenearrow_forwardMenthene, a compound found in mint plants, has the formula C10H18 and the IUPAC name 1-isopropyl- 4-methylcyclohexene. What is the structure of menthene?arrow_forward
- Glucose, C6H12O6, contains an aldehyde group but exist predominantly in the form of the cyclic hemiacetal show below. A cyclic hemiacetal is formed when the —OH group of one carbon bonds to the carbonyl group of another carbon. Identify which carbon provides the —OH group and which provides the —CHO? Give a functional isomer of glucose and draw its structure.arrow_forwardEthers (general formula R—O—R)have many important uses. Until recently,methyl tert-butyl ether (MTBE, right)was used as an octane booster and fueladditive for gasoline. It increases the oxy-gen content of the fuel, which reducesCO emissions. MTBE is synthesized bythe catalyzed reaction of 2-methylpropene with methanol.(a) Write a balanced equation for the synthesis of MTBE. (Hint:Alcohols add to alkenes similarly to the way water does.)(b) If the government required that auto fuel mixtures contain2.7% oxygen by mass to reduce CO emissions, how many gramsof MTBE would have to be added to each 100. g of gasoline?(c) How many liters of MTBE would be in each liter of fuel mix-ture? (The density of both gasoline and MTBE is 0.740 g/mL.)(d) How many liters of air (21% O₂ by volume) are needed at24C and 1.00 atm to fully combust 1.00 L of MTBE?arrow_forward4 But-2-enal, CH₂CH=CHCHO, is a pale yellow, flammable liquid with an irritating odour. (a) But-2-enal exists as two stereoisomers. Draw skeletal formulae to show the structure of the two stereoisomers of but-2-enal. (b) (i) Describe a simple chemical test that would show that but-2-enal is an aldehyde. (ii) Explain why this test gives a different result with aldehydes than it does with keton (c) But-2-enal also reacts with sodium borohydride, NaBH4. (i) Identify the organic compound formed in this reaction. (ii) State the type of chemical reaction occurring. (d) Precautions must be taken to prevent but-2-enal catching fire. Construct a balanced equation for the complete combustion of but-2-enal, C₂HO.arrow_forward
- Name and draw a structural formula for the major product of each alkene addition reaction: CH S (a) CH₂C=CH₂ + HI →→→→ (b) CH 3 + HClarrow_forward(a) which a disubstituted cis- alkene? (b) which is the geometric isomer of D? (c) which is a tri-substituted Z- alkene? (d) which is the most stable alkene? (e) which has the highest boiling point? (f) which has the highest MP?arrow_forwardDraw structures that fit each description and name the functional group in each molecule: (a) two constitutional isomers with molecular formula C5H10O that contain different functional groups; (b) two constitutional isomers with molecular formula C6H10O that contain the same functional group.arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning