
Concept explainers
(a)
Interpretation:
The Lewis structure for cyclopropane having molecular formula C3 H6 is to be drawn.
Concept Introduction:
During the formation of a compound each atom tends to lose, gain or share enough electrons to achieve an electronic configuration having eight valence electrons. This rule is also known as octet rule. The number of electrons present in outermost shell of an atom which are available for bonding are known as valence electrons. For a molecule, total number of valence electrons will be sum of valence electrons of each atom present in the molecule.
A Lewis structure is representation of distribution of electrons on each atom of the molecule. Some of the electrons are shared by atoms to form bonds and some exist as lone pair which do not take part in bonding.
(b)
Interpretation:
Using VSEPR Theory, the geometry of each central atom present in given structure of Cyclopropane is to be identified.
Concept Introduction:
Bond angles in the molecules can be predicted by using valence shell electron pair repulsion (VSEPR) model. According to this model, the valence electrons of an atom are involved in the formation of single, double or triple bond. The valence electrons can also be unshared and exist as lone pair on atoms. The combination forms a negatively charged region of electron density around a nucleus. Since, like charges do not attract, the region of electron density around a nucleus spread out so that each atom is as far away from each other at different angles.
(c)
Interpretation:
Using VSEPR theory, the various relative bond angles associated with each central atom of the Cyclopropane molecule is to be determined.
Concept Introduction:
Bond angles in the molecules can be predicted by using valence shell electron pair repulsion (VSEPR) model. According to this model, the valence electrons of an atom are involved in the formation of single, double or triple bond. The valence electrons can also be unshared and exist as lone pair on atoms. The combination forms a negatively charged region of electron density around a nucleus. Since, like charges do not attract, the region of electron density around a nucleus spread out so that each atom is as far away from each other at different angles.
(d)
Interpretation:
Observing the given the shape and size of the Cyclopropane ring, the bond angle for C−C−C is to be predicted.
Concept Introduction:
Bond angle of the molecules can be predicted by using valence shell electron pair repulsion (VSEPR) model.
(e)
Interpretation:
A proper explanation with reason is to be given, why cyclopropane is considerably less stable than other three-carbon compounds that do not contain a ring.
Concept Introduction:
Bond angle of the molecules can be predicted by using valence shell electron pair repulsion (VSEPR) model.

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Chapter 3 Solutions
Bundle: Introduction to General, Organic and Biochemistry, 11th + OWLv2, 4 terms (24 months) Printed Access Card
- 1. Show the steps necessary to make 2-methyl-4-nonene using a Wittig reaction. Start with triphenylphosphine and an alkyl halide. After that you may use any other organic or inorganic reagents. 2. Write in the product of this reaction: CH3 CH₂ (C6H5)₂CuLi H₂O+arrow_forward3. Name this compound properly, including stereochemistry. H₂C H3C CH3 OH 4. Show the step(s) necessary to transform the compound on the left into the acid on the right. Bri CH2 5. Write in the product of this LiAlH4 Br H₂C OHarrow_forwardWhat are the major products of the following reaction? Please provide a detailed explanation and a drawing to show how the reaction proceeds.arrow_forward
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- Can u help me figure out the reaction mechanisms for these, idk where to even startarrow_forwardHi, I need your help with the drawing, please. I have attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forwardHi, I need your help i dont know which one to draw please. I’ve attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forward
- 5. Write the formation reaction of the following complex compounds from the following reactants: 6. AgNO₃ + K₂CrO₂ + NH₄OH → 7. HgNO₃ + excess KI → 8. Al(NO₃)₃ + excess NaOH →arrow_forwardIndicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. CO₂C2H5 + CH3-NH-NH,arrow_forwardDraw the major product of this reaction N-(cyclohex-1-en-1-yl)-1-(pyrrolidino) reacts with CH2=CHCHO, heat, H3O+arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
