(a)
Interpretation: The shortest
Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order, shorter is the bond length.
Answer to Problem 1.68P
The shortest
Explanation of Solution
In hybridization, one
Figure 1
Both
The shortest
(b)
Interpretation: The longest
Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.
Answer to Problem 1.68P
The longest
Explanation of Solution
In hybridization, one
The longest
(c)
Interpretation: The shortest
Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.
Answer to Problem 1.68P
The shortest
Explanation of Solution
In hybridization, one
The shortest
(d)
Interpretation: The weakest
Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.
Answer to Problem 1.68P
The weakest
Explanation of Solution
In hybridization, one
Both
The weakest
(e)
Interpretation: The strongest
Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.
Answer to Problem 1.68P
The strongest
Explanation of Solution
The length and strength of a
Triple bond is formed by
The strongest
(f)
Interpretation: Bond
Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.
Answer to Problem 1.68P
Bond
Explanation of Solution
In hybridization, one
Bond
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Chapter 1 Solutions
PKG ORGANIC CHEMISTRY
- A DEPT NMR spectrum is shown for a molecule with the molecular formula of C5H12O. Draw the structure that best fits this data. 200 180 160 140 120 100 一盆 00 40 8- 20 ppm 0 Qarrow_forwardDon't used hand raitingarrow_forwardShown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H. H. +N=C H H H Cl: Click and drag to start drawing a structure. : ? g B S olo Ar B Karrow_forward
- Don't used hand raitingarrow_forwardS Shown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H H = HIN: H C. :0 H /\ H H Click and drag to start drawing a structure. ×arrow_forwardPlease help me figure out these calculation and what should be plotted. These are notes for my chemistry class.arrow_forward
- Nonearrow_forwardNonearrow_forwardPart II. two unbranched ketone have molecular formulla (C8H100). El-ms showed that both of them have a molecular ion peak at m/2 =128. However ketone (A) has a fragment peak at m/2 = 99 and 72 while ketone (B) snowed a fragment peak at m/2 = 113 and 58. 9) Propose the most plausible structures for both ketones b) Explain how you arrived at your conclusion by drawing the Structures of the distinguishing fragments for each ketone, including their fragmentation mechanisms.arrow_forward
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