ORGANIC CHEM.(LL)W/STD GDE.+CONNECT PKG
ORGANIC CHEM.(LL)W/STD GDE.+CONNECT PKG
5th Edition
ISBN: 9781260858129
Author: SMITH
Publisher: MCG
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Chapter 1, Problem 1.65P
Interpretation Introduction

(a)

Interpretation: The orbitals used to form the highlighted bonds are to be predicted.

Concept introduction: Hybridization is the combination of two or more atomic orbitals to form the same number of hybrid orbitals, each having the same shape and energy.

Expert Solution
Check Mark

Answer to Problem 1.65P

Orbitals used in the formation of given bonds are:

[1]Csp2H1s[2]Csp2Csp2[3]Csp2Csp3

Explanation of Solution

The given compound is,

ORGANIC CHEM.(LL)W/STD GDE.+CONNECT PKG, Chapter 1, Problem 1.65P , additional homework tip  1

Figure 1

In bond [1], there are three groups around C and no lone pair. Thus, it is sp2 hybridized. This bond is formed from Csp2H1s orbitals. In bond [2], there are three groups around each C and no lone pair. Thus, it is sp2 hybridized. This bond is formed from Csp2Csp2. In bond [3], there are three groups around C(II) and no lone pair. Thus, it is sp2 hybridized. And there are four groups around C(III) and no lone pair. Thus, it is sp3 hybridized. This bond is formed from Csp2Csp3.

Conclusion

Orbitals used in the formation of given bonds are:

[1]Csp2H1s[2]Csp2Csp2[3]Csp2Csp3

Interpretation Introduction

(b)

Interpretation: The orbitals used to form the highlighted bonds are to be predicted.

Concept introduction: Hybridization is the combination of two or more atomic orbitals to form the same number of hybrid orbitals, each having the same shape and energy.

Expert Solution
Check Mark

Answer to Problem 1.65P

Orbitals used in the formation of given bonds are:

[1]Csp3Csp2[2]Csp2Osp2

Explanation of Solution

ORGANIC CHEM.(LL)W/STD GDE.+CONNECT PKG, Chapter 1, Problem 1.65P , additional homework tip  2

Figure 2

In bond [1], there are four groups around C(I) including two hydrogen atoms and no lone pair. Thus, it is sp3 hybridized. This bond is formed from Csp3Csp2 orbitals. In bond [2], there are three groups around C and no lone pair. Thus, it is sp2 hybridized. And there is one group and two lone pairs around O. Thus, it is sp2 hybridized. This bond is formed from Csp2Osp2 orbitals.

Conclusion

Orbitals used in the formation of given bonds are:

[1]Csp3Csp2[2]Csp2Osp2.

Interpretation Introduction

(c)

Interpretation: The orbitals used to form the highlighted bonds are to be predicted.

Concept introduction: Hybridization is the combination of two or more atomic orbitals to form the same number of hybrid orbitals, each having the same shape and energy.

Expert Solution
Check Mark

Answer to Problem 1.65P

Orbitals used in the formation of given bonds are:

[1]H1sCsp[2]CspCsp,[3]CspCsp2and [4]Nsp2Csp3

Explanation of Solution

ORGANIC CHEM.(LL)W/STD GDE.+CONNECT PKG, Chapter 1, Problem 1.65P , additional homework tip  3

Figure 3

In bond [1], there are two groups around C(I), including one hydrogen atom and triply bonded C atom. Thus, it is sp hybridized. This bond is formed from H1s-Csp orbitals. In bond [2], there are two groups around each C atom. Thus, it is sp hybridized. This bond is formed from CspCsp orbitals. In bond [3], there are two groups around C(II) atom. Thus, it is sp hybridized. And there three groups around C(III) including one hydrogen atom. Thus, it is sp2 hybridized This bond is formed from CspCsp2 orbitals. In bond [4], there are two groups around N atom and one lone pair. Thus, it is sp2 hybridized. And there are four groups around C including three hydrogen atoms. Thus, it is sp3 hybridized. This bond is formed from Nsp2Csp3 orbitals.

Conclusion

(a) [1]H1sCsp[2]CspCsp,[3]CspCsp2and [4]Nsp2Csp3

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Chapter 1 Solutions

ORGANIC CHEM.(LL)W/STD GDE.+CONNECT PKG

Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Prob. 1.13PCh. 1 - Draw a second resonance structure for each species...Ch. 1 - Prob. 1.15PCh. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Using the principles of VSEPR theory, you can...Ch. 1 - Convert each condensed formula to a Lewis...Ch. 1 - Prob. 1.21PCh. 1 - Prob. 1.22PCh. 1 - Convert each skeletal structure to a complete...Ch. 1 - What is the molecular formula of quinine, the...Ch. 1 - Draw in all hydrogens and lone pairs on the...Ch. 1 - Prob. 1.26PCh. 1 - What orbitals are used to form each of the CC, and...Ch. 1 - What orbitals are used to form each bond in the...Ch. 1 - Determine the hybridization around the highlighted...Ch. 1 - The unmistakable odor of a freshly cut cucumber is...Ch. 1 - Prob. 1.31PCh. 1 - Rank the following atoms in order of increasing...Ch. 1 - Prob. 1.33PCh. 1 - Prob. 1.34PCh. 1 - Provide the following information about...Ch. 1 - Use the ball-and-stick model to answer each...Ch. 1 - Citric acid is responsible for the tartness of...Ch. 1 - Zingerone gives ginger its pungent taste. a.What...Ch. 1 - Assign formal charges to each carbon atom in the...Ch. 1 - Assign formal charges to each and atom in the...Ch. 1 - Prob. 1.41PCh. 1 - Prob. 1.42PCh. 1 - Prob. 1.43PCh. 1 - Draw all possible isomers for each molecular...Ch. 1 - 1.45 Draw Lewis structures for the nine isomers...Ch. 1 - Prob. 1.46PCh. 1 - Prob. 1.47PCh. 1 - Prob. 1.48PCh. 1 - Prob. 1.49PCh. 1 - Prob. 1.50PCh. 1 - Prob. 1.51PCh. 1 - Prob. 1.52PCh. 1 - Consider compounds A-D, which contain both a...Ch. 1 - Prob. 1.54PCh. 1 - Prob. 1.55PCh. 1 - 1.56 Consider the compounds and ions with curved...Ch. 1 - 1.57 Predict all bond angles in each...Ch. 1 - 1.58 Predict the geometry around each highlighted...Ch. 1 - Prob. 1.59PCh. 1 - Draw in all the carbon and hydrogen atoms in each...Ch. 1 - 1.61 Convert each molecule into a skeletal...Ch. 1 - Prob. 1.62PCh. 1 - Prob. 1.63PCh. 1 - Predict the hybridization and geometry around each...Ch. 1 - Prob. 1.65PCh. 1 - Ketene, , is an unusual organic molecule that has...Ch. 1 - Rank the following bonds in order of increasing...Ch. 1 - Prob. 1.68PCh. 1 - Two useful organic compounds that contain Cl atoms...Ch. 1 - Use the symbols + and to indicate the polarity of...Ch. 1 - Prob. 1.71PCh. 1 - Anacin is an over-the-counter pain reliever that...Ch. 1 - Answer the following questions about acetonitrile...Ch. 1 - Prob. 1.74PCh. 1 - 1.75 The principles of this chapter can be...Ch. 1 - a. What is the hybridization of each N atom in...Ch. 1 - 1.77 Stalevo is the trade name for a medication...Ch. 1 - 1.78 and are two highly reactive carbon...Ch. 1 - 1.79 The N atom in (acetamide) is hybridized,...Ch. 1 - Prob. 1.80PCh. 1 - Prob. 1.81PCh. 1 - Prob. 1.82PCh. 1 - Prob. 1.83PCh. 1 - Prob. 1.84PCh. 1 - Prob. 1.85P
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