Concept explainers
(a)
Interpretation:
Sigma and pi bond in
Concept Introduction:
Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.
Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Geometry of different types of molecule with respect to the hybridizations are mentioned below,
(a)

Explanation of Solution
Given molecule is
The Lewis electron dot structure for
.
Sigma bond and pi bonds in the molecule are marked below:
(b)
Interpretation:
Sigma and pi bond in
Concept Introduction:
Refer to (a).
(b)

Explanation of Solution
Given molecule is
The Lewis electron dot structure for
.
Sigma bond and pi bonds in the molecule are marked below:
(c)
Interpretation:
Sigma and pi bond in
Concept Introduction:
Refer to (a).
(c)

Explanation of Solution
Given molecule is
The Lewis electron dot structure for
.
Sigma bond and pi bonds in the molecule are marked below:
(d)
Interpretation:
Sigma and pi bond in
Concept Introduction:
Refer to (a).
(d)

Explanation of Solution
Given molecule is
The Lewis electron dot structure for
Sigma bond and pi bonds in the molecule are marked below:
Want to see more full solutions like this?
Chapter 7 Solutions
OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
- At 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Without using graphs, calculate the order of the reaction. t/s [R]/(mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forwardPredict the organic products that form in the reaction below, and draw the skeletal ("line") structures of the missing organic products. Please include all steps & drawings & explanations.arrow_forwardWhat are the missing reagents for the spots labeled 1 and 3? Please give a detailed explanation and include the drawings and show how the synthesis proceeds with the reagents.arrow_forward
- What are the products of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forwardWhat would happen if you added the HCI to the Grignard reagent before adding benzophenone? Draw a reaction mechanism to support your answer.arrow_forwardAt 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Calculate the order of the reaction. t/s [R]/ (mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forward
- Write the correct IUPAC names of the molecules in the picturearrow_forwardHow many grams of solid NaCN have to be added to 1.5L of water to dissolve 0.18 mol of Fe(OH)3 in the form Fe(CN)63 - ? ( For simplicity, ignore the reaction of CN - ion with water) Ksp for Fe(OH)3 is 2.8E -39, and Kform for Fe(CN)63 - is 1.0E31arrow_forwardDraw the most stable chair conformation of 1-ethyl-1-methylcyclohexane, clearly showing the axial and equatorial substituents. [4] Draw structures corresponding to the following IUPAC name for each of the following compounds; [5] i) 4-Isopropyl-2,4,5-trimethylheptane ii) trans-1-tert-butyl-4-ethylcyclohexane iii) Cyclobutylcycloheptane iv) cis-1,4-di-isopropylcyclohexane (chair conformation) v) 3-Ethyl-5-isobutylnonanearrow_forward
- Draw and name molecules that meet the following descriptions; [4] a) An organic molecule containing 2 sp2 hybridised carbon and 1 sp-hybridised carbon atom. b) A cycloalkene, C7H12, with a tetrasubstituted double bond. Also answer question 2 from the imagearrow_forwardH 14. Draw the line angle form of the following molecule make sure you use the proper notation to indicate spatial positioning of atoms. F F H 15. Convert the following condensed form to line angle form: (CH3)3CCH2COCH2CON(CH2CH3)2arrow_forwardIn a reaction between two reactants A and B, the half-life is the same for both only if(A) the stoichiometry A:B is 1:1.(B) the stoichiometry A:B is 1:2 or 2:1.arrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning

