Compare the estimated values with the experimental values have to be done. Concept Introduction: Atomic radius: The concept explain chemical element is a measured of the size of its atoms, in other words to measure the distance from the center of the nucleus to the boundary of the surrounding cloud of number of electrons. Bond distance: In molecular geometry, bond length or bond distance is the average distance between nuclei of two bonded atoms in a molecule. It is a transferable property of a bond between atoms of fixed types, relatively independent of the rest of the molecule. Increase and decrease electro negativity: The less vacancy electrons an atoms has the least it will gain of electrons. Moreover the electron affinity decrease down the groups and from right to left across the periods on the periodic table, the reason is electrons are placed in a higher energy level far from the nucleus thus a decrease from its pull.

Question

Want to see the full answer?

Answer 1

Question

Chapter 7, Problem 68SCQ

Interpretation Introduction

Interpretation:

Compare the estimated values with the experimental values have to be done.

Concept Introduction:

Atomic radius: The concept explain chemical element is a measured of the size of its atoms, in other words to measure the distance from the center of the nucleus to the boundary of the surrounding cloud of number of electrons.

Bond distance: In molecular geometry, bond length or bond distance is the average distance between nuclei of two bonded atoms in a molecule. It is a transferable property of a bond between atoms of fixed types, relatively independent of the rest of the molecule.

Increase and decrease electro negativity: The less vacancy electrons an atoms has the least it will gain of electrons. Moreover the electron affinity decrease down the groups and from right to left across the periods on the periodic table, the reason is electrons are placed in a higher energy level far from the nucleus thus a decrease from its pull.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Done 11:14 ⚫ worksheets.beyondlabz.com 5 (a). Using the peak information you listed in the tables for both structures, assign each peak to that portion of the structure that produces the peak in the NMR spectrum. Draw this diagram on your own sheet of paper and attach the sketch of your drawing to this question. Question 6 5 (b). Using the peak information you listed in the tables for both structures, assign each peak to that portion of the structure that produces the peak in the NMR spectrum. Draw this diagram on your own sheet of paper and attach the sketch of your drawing to this question. Question 7 6. Are there any differences between the spectra you obtained in Beyond Labz and the predicted spectra? If so, what were the differences? <

2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled** Peak Chemical Shift (d) 5.7 1 Multiplicity multiplate .......... 5.04 double of doublet 2 4.98 double of doublet 3 4.05 doublet of quartet 4 5 LO 3.80 quartet 1.3 doublet 6 Peak Chemical Shift (d) Multiplicity

Interpreting NMR spectra is a skill that often requires some amount of practice, which, in turn, necessitates access to a collection of NMR spectra. Beyond Labz Organic Synthesis and Organic Qualitative Analysis have spectral libraries containing over 700 1H NMR spectra. In this assignment, you will take advantage of this by first predicting the NMR spectra for two closely related compounds and then checking your predictions by looking up the actual spectra in the spectra library. After completing this assignment, you may wish to select other compounds for additional practice. 1. Write the IUPAC names for the following two structures: Question 2 Question 3 2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled**