Concept explainers
17-9 Answer true or false.
(a) The one aldehyde and the one ketone with a molecular formula of C3H6O are constitutional isomers.
(b)
(c) The VSEPR model predicts bond angles of 1200 about the carbonyl carbon of aldehydes and ketones.
(d) The carbonyl carbon of a ketone is a stereocenter.
(a)

Interpretation:
Answer true or false for the following statement.
The one aldehyde and one ketone with a molecular formula of
Concept Introduction:
Constitutional isomers have the same molecular formula but different structural formulas or connectivity with atoms is different. In aldehydes, the carbonyl group is bonded to a hydrogen atom and ketones carbonyl group is bonded to two carbon atoms.
Answer to Problem 1P
The one aldehyde and one ketone with a molecular formula of
Explanation of Solution
The given molecular formula:
For this molecular formula we can draw both aldehyde and ketone. They are as follows.
From the above structures aldehydes and ketones having same molecular formula are constitutional isomers.
Therefore, the given statement is true.
(b)

Interpretation:
Answer true or false for the following statement.
Aldehydes and ketones both contain a carbonyl group.
Concept Introduction:
In aldehydes, the carbonyl group is bonded to a hydrogen atom and ketones carbonyl group is bonded to two carbon atoms.
Answer to Problem 1P
Aldehydes and ketones both contain a carbonyl group is true statement.
Explanation of Solution
In aldehydes, the carbonyl group is bonded to a hydrogen atom and in ketone carbonyl group is bonded to two carbon atoms. Hence, both an aldehyde and a ketone have a carbonyl group.
Where, R is an alkyl group.
Therefore, the given statement is true.
(c)

Interpretation:
Answer true or false for the following statement.
The VSEPR model predicts bond angles of 1200 about the carbonyl carbon of aldehydes and ketones.
Concept Introduction:
In aldehydes, the carbonyl group is bonded to a hydrogen atom and ketones carbonyl group is bonded to two carbon atoms. VSEPR model predicts the geometry of the molecule with the help of number of pair of electrons present around the central atoms and bond angle of the molecule.
Answer to Problem 1P
The VSEPR model predicts bond angles of 1200 about the carbonyl carbon if aldehydes and ketones is the true statement.
Explanation of Solution
In aldehydes, the carbonyl group is bonded to a hydrogen atom and ketones carbonyl group is bonded to two carbon atoms. The carbonyl group of aldehyde and ketone are represented are as follows.
According to VSEPR theory, three pair of electron groups forms a Trigonal planar geometry with bond angle of 1200.
Therefore, the given statement is true.
(d)

Interpretation:
Answer true or false for the following statement.
The carbonyl carbon of ketone is a stereocentre.
Concept Introduction:
A stereocentre is a tetrahedral carbon atom in which four different groups are attached to it. When an atom generally carbon is linked with four different groups, then that centre is known as chiral centre.
Answer to Problem 1P
The carbonyl carbon of ketone is a stereocenter is the false statement.
Explanation of Solution
In aldehydes, the carbonyl group is bonded to a hydrogen atom and in ketone carbonyl group is bonded to two carbon atoms. The carbonyl group of aldehyde and ketone are represented are as follows.
In ketones, the carbonyl carbon is boded to carbonyl oxygen by a double bond group and bonded to two other carbon atoms.
Therefore, the given statement is false.
Want to see more full solutions like this?
Chapter 16 Solutions
Introduction to General, Organic and Biochemistry
- Q1: Answer the questions for the reaction below: ..!! Br OH a) Predict the product(s) of the reaction. b) Is the substrate optically active? Are the product(s) optically active as a mix? c) Draw the curved arrow mechanism for the reaction. d) What happens to the SN1 reaction rate in each of these instances: 1. Change the substrate to Br "CI 2. Change the substrate to 3. Change the solvent from 100% CH3CH2OH to 10% CH3CH2OH + 90% DMF 4. Increase the substrate concentration by 3-fold.arrow_forwardExperiment 27 hates & Mechanisms of Reations Method I visual Clock Reaction A. Concentration effects on reaction Rates Iodine Run [I] mol/L [S₂082] | Time mo/L (SCC) 0.04 54.7 Log 1/ Time Temp Log [ ] 13,20] (time) / [I] 199 20.06 23.0 30.04 0.04 0.04 80.0 22.8 45 40.02 0.04 79.0 21.6 50.08 0.03 51.0 22.4 60-080-02 95.0 23.4 7 0.08 0-01 1970 23.4 8 0.08 0.04 16.1 22.6arrow_forward(15 pts) Consider the molecule B2H6. Generate a molecular orbital diagram but this time using a different approach that draws on your knowledge and ability to put concepts together. First use VSEPR or some other method to make sure you know the ground state structure of the molecule. Next, generate an MO diagram for BH2. Sketch the highest occupied and lowest unoccupied MOs of the BH2 fragment. These are called frontier orbitals. Now use these frontier orbitals as your basis set for producing LGO's for B2H6. Since the BH2 frontier orbitals become the LGOS, you will have to think about what is in the middle of the molecule and treat its basis as well. Do you arrive at the same qualitative MO diagram as is discussed in the book? Sketch the new highest occupied and lowest unoccupied MOs for the molecule (B2H6).arrow_forward
- Q8: Propose an efficient synthesis of cyclopentene from cyclopentane.arrow_forwardQ7: Use compound A-D, design two different ways to synthesize E. Which way is preferred? Please explain. CH3I ONa NaOCH 3 A B C D E OCH3arrow_forwardPredict major product(s) for the following reactions. Note the mechanism(s) of the reactions (SN1, E1, SN2 or E2).arrow_forward
- (10 pts) The density of metallic copper is 8.92 g cm³. The structure of this metal is cubic close-packed. What is the atomic radius of copper in copper metal?arrow_forwardPredict major product(s) for the following reactions. Note the mechanism(s) of the reactions (SN1, E1, SN2 or E2).arrow_forwardPredict major product(s) for the following reactions. Note the mechanism(s) of the reactions (SN1, E1, SN2 or E2).arrow_forward
- Q3: Rank the following compounds in increasing reactivity of E1 and E2 eliminations, respectively. Br ca. go do A CI CI B C CI Darrow_forwardQ5: Predict major product(s) for the following reactions. Note the mechanism(s) of the reactions (SN1, E1, SN2 or E2). H₂O דיי "Br KN3 CH3CH2OH NaNH2 NH3 Page 3 of 6 Chem 0310 Organic Chemistry 1 HW Problem Sets CI Br excess NaOCH 3 CH3OH Br KOC(CH3)3 DuckDuckGarrow_forwardQ4: Circle the substrate that gives a single alkene product in a E2 elimination. CI CI Br Brarrow_forward
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning





