(a)
Interpretation:
The differences in the structural formula of testosterone and methandrostenolone should be determined along with
Concept Introduction:
Steroids are the third major class of lipids. These are the compounds containing the following ring system:

Answer to Problem 70P
Both methandrostenolone and testosterone hormone contains hydroxyl functional group (alcohol) and carbonyl functional group (kentone).
In the structural formula of testosterone hormone, there is only one double bond and it has only one methyl group attached to cyclopentane ring whereas in methandrostenolone there are two double bonds and two methyl groups are attached to the cyclopentane ring.
Explanation of Solution
Testosterone and methandrostenolone both the hormones contain one −OH group attached to cyclopentane ring and one >C=O group in cyclohexene ring. Therefore both alcoholic and
In the structure of testosterone there is only a double bond in cyclohexene ring having ketonic group and no methyl group is present on the carbon of cyclopentane ring having alcoholic group as shown:
In the structure of methandrostenolone, there are two double bonds in cyclohexene ring having ketonic group and one methyl group attached on the carbon of cyclopentane ring having alcoholic group as shown:
(b)
Interpretation:
In both the given hormones mark all the stereocenters and state the number of stereoisomer possible for each.
Concept Introduction:
Stereoisomers are the compounds that are differ only in the spatial arrangement of their atoms. Each stereoisomer has at least one stereocenter. A stereocenter is a tetrahedral carbon atom that has four different groups bonded to it. For a molecule with n sterocenters, a maximum of

Answer to Problem 70P
Stereocenters in testosterone:
Since testosterone has six stereocenters therefore it has 64 possible stereoisomers.
Stereocenters in methandrostenolone:
Since methandrostenolone has six stereocenters therefore it has 64 possible stereoisomers.
Explanation of Solution
A stereocenter is a tetrahedral carbon atom that has four different groups bonded to it.
Stereocenters in testosterone:
In testosterone there are six stereocenters.
For a molecule with n stereocenter, a maximum of
Stereocenters in methandrostenolone:
In methandrostenolone there are six stereocenters.
For a molecule with n stereocenter, a maximum of
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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
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning

