Answered step by step
Verified Expert Solution
Link Copied!

Question

1 Approved Answer

(i) Calculate the double bond equivalents (DBE) for each molecule. (ii) Assign the 'H NMR spectra completely, rationalise the number of peaks, relative integral,

(i) Calculate the double bond equivalents (DBE) for each molecule. (ii) Assign the 'H NMR spectra completely, rationalise the number of peaks, relative integral, their multiplicity or splitting pattern where appropriate. (iii) Rationalise the 13C NMR spectra. (iv) Rationalise all numbered peaks in the mass spectra and IR spectra. (v) Provide a brief logical explanation for how you arrived at unambiguous structures for compounds A and B. Problem 88 2114 3295 IR Spectrum diquid fam 2000 1600 v (am) 4000 3000 1200 800 10 Mass Spectrum 52 80 60 No significant UV absorption above 220 nm 20 40 80 120 160 200 240 260 m/e 13C NMR Spectrum (100.0 MHe. CDCI, sciution) DEPT O CH CHt solvent proton decoupied 200 160 120 80 40 8 (ppm) H NMR Spectrum (400 MHz. CDa, cluion Exchanges with Dyo expansion 2H 2H 1H 2H 2H TMS 25 2.0 3 1 8 (ppm) 10 4 2 ed ose

Step by Step Solution

3.47 Rating (160 Votes )

There are 3 Steps involved in it

Step: 1

blur-text-image

Get Instant Access to Expert-Tailored Solutions

See step-by-step solutions with expert insights and AI powered tools for academic success

Step: 2

blur-text-image

Step: 3

blur-text-image

Ace Your Homework with AI

Get the answers you need in no time with our AI-driven, step-by-step assistance

Get Started

Recommended Textbook for

Organic Chemistry

Authors: Paula Yurkanis Bruice

4th edition

131407481, 978-0131407480

More Books

Students also viewed these Chemistry questions