The possible structure for the compound C 6 H 15 N that exhibits two types of signals in its proton NMR spectrum and two signals in 13 C NMR spectrum has to be drawn. Concept introduction: The arrangement of atoms that are bonded together determines its constitution and molecular formula of that particular compound. This concept is referred as structural isomers or in more modern term constitutional isomers. Each atom has a typical valency or valence which is defined as the ability of an atom to form a chemical bond with other atoms. For example, carbon has four valence or tetravalent that means carbon has the capacity to form four bonds with other elements or other atoms. Nitrogen atoms are trivalent whereas hydrogen atoms are monovalent in nature. In proton NMR, the signals are based on the arrangement of hydrogen atoms that are connected to carbon atoms. In 13 C NMR, the signals are based on the arrangement of carbon atoms. To find: Draw the possible structure for the compound C 6 H 15 N that exhibits two types of signals in its proton NMR spectrum and two signals in 13 C NMR spectrum Find the valency for carbon (C), hydrogen (H) and nitrogen (N) in C 6 H 15 N

Question

Want to see the full answer?

Answer 1

Question

Chapter 23, Problem 83IP

Interpretation Introduction

Interpretation: The possible structure for the compound C₆H₁₅N that exhibits two types of signals in its proton NMR spectrum and two signals in ¹³C NMR spectrum has to be drawn.

Concept introduction:

The arrangement of atoms that are bonded together determines its constitution and molecular formula of that particular compound. This concept is referred as structural isomers or in more modern term constitutional isomers. Each atom has a typical valency or valence which is defined as the ability of an atom to form a chemical bond with other atoms. For example, carbon has four valence or tetravalent that means carbon has the capacity to form four bonds with other elements or other atoms. Nitrogen atoms are trivalent whereas hydrogen atoms are monovalent in nature.

In proton NMR, the signals are based on the arrangement of hydrogen atoms that are connected to carbon atoms. In ¹³C NMR, the signals are based on the arrangement of carbon atoms.

To find: Draw the possible structure for the compound C₆H₁₅N that exhibits two types of signals in its proton NMR spectrum and two signals in ¹³C NMR spectrum

Find the valency for carbon (C), hydrogen (H) and nitrogen (N) in C₆H₁₅N

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Speaking of composite materials, indicate the correct option:(A). Composite materials can only be: metal-polymer or polymer-polymer.(B). Composite materials can be made up of particles, but not fibers or sheets.(C). When the reinforcing particles are uniformly distributed in a composite material, there may be a greater tendency for it to have isotropic properties.(D). None of the above is correct.

If we are talking about viscoelastic modulus or viscoelastic relaxation modulus in polymers, indicate the correct option.(A). It reports the variation of elastic behavior as a function of time.(B). It is only useful for defining its glass transition temperature.(C). It only allows us to define the polymer degradation temperature.(D). Neither option is correct.

When natural light falls perpendicularly on a material A, it has a reflectivity of 0.813%. Indicate the value of the refractive index.