Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter SRP, Problem 28P

Compound Y ( C 6 H 14 O ) shows prominent IR absorption bands at 3334 (broad), 2963, 1463, 1381, and 1053 cm−-1. The broadband proton-decoupled 13 C NMR spectrum of Y is given in Fig. 1. Propose a structure for Y.

Chapter SRP, Problem 28P, 28.	Compound Y  shows prominent IR absorption bands at 3334 (broad), 2963, 1463, 1381, and 1053

Figure 1 The broadband proton-decoupled 13 C NMR spectra of compounds Y (Problem 28) and Z (Problem 29). Information from the DEPT 13 C NMR spectra is given above the peaks.

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Finish the reactions  hand written please
Part A Identify each alcohol as primary, secondary, or tertiary Drag the appropriate items to their respective bins. CH₂ H₂C- -C-OH HO CH₂ Primary Он OH CH₂ OH CCH₂OH CH₂ сн Secondary Tertiary Reset Help CH,CH₂ (CH)CHCH,OH CH,CH,CH,CCH, CHOH CH₂ Different types of alcohol groups Alcohol and its reaction: 8. Combing two alcohol molecules below and completing the reaction with Product .( Hint Reaction called etherification as ether is formed and name the ether once you complete the reaction. Hint.: R-O-H+H-O-RR-O-R Do the reaction: CH₂OH + CH₂OH---→ + H-O-H 9. Write the reaction of formation of alcohol from alkene by adding water: Addition reaction also called hydration reaction as we are adding water which occur always in presence of acid Hint: Break the double bond and add H and OH if symmetrical then add anywhere if unsymmetrical then follow Markovnikov rule H should go to that double bone carbon which has more hydrogen CH2=CH2 + H₂O-→
Complete the reaction    hand written please

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