Drag the appropriate labels to their respective targets. Note: not all labels can be used. σC(sp²) - H(s) σC(sp) - H(s) oC(sp) - N(px) C(sp) - N(py) σC(sp) - N(p₂) TC(px) - N(px) С(Py) – N(Py) TС(p₂) - N(p₂) H N. y

Drag the appropriate labels to their respective targets. Note: not all labels can be used. σC(sp²) - H(s) σC(sp) - H(s) oC(sp) - N(px) C(sp) - N(py) σC(sp) - N(p₂) TC(px) - N(px) С(Py) – N(Py) TС(p₂) - N(p₂) H N. y

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy

Section13.SE: Something Extra

Problem 33AP

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Concept explainers

Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.

Question

Drag the appropriate labels to their respective targets. Note: not all labels can be used.
σC(sp²) - H(s)
σC(sp) - H(s)
oC(sp) - N(px)
C(sp) - N(py)
σC(sp) – N(pz)
TС(px) - N(px)
TС(Py) - N(Py)
TС(p₂) - N(p₂)
H
N

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