AP Notes, Outlines, Study Guides, Vocabulary, Practice Exams and more!

Hemiacetal

Organic Chemistry Lecture 18

Subject: 
Chemistry
Rating: 
0
No votes yet
SocialTags: 
Chemistry
Organic chemistry
Functional groups
Ketone
Carbonyl group
Aldehyde
Grignard reaction
Wittig reaction
Hemiacetal
Acetal
Alkene
Alcohol

Chapter 18 ?2010, Prentice Hall Organic Chemistry, 7th Edition L. G. Wade, Jr. Ketones and Aldehydes Chapter 18 * Carbonyl Compounds Chapter 18 Chapter 18 * Carbonyl Structure Carbon is sp2 hybridized. C?O bond is shorter, stronger, and more polar than C?C bond in alkenes. Chapter 18 Chapter 18 * Ketone Nomenclature Number the chain so that carbonyl carbon has the lowest number. Replace the alkane -e with -one. 3-methyl-2-butanone 4-hydroxy-3-methyl-2-butanone C H 3 C O C H C H 3 C H 3 C H 3 C O C H C H 3 C H 2 O H 1 2 3 4 1 2 3 4 Chapter 18 Chapter 18 * Ketone Nomenclature (Continued) For cyclic ketones, the carbonyl carbon is assigned the number 1. 3-bromocyclohexanone O B r 1 3 Chapter 18 Chapter 18 * C H 3 C H 2 C H C H 3 C H 2 C H O Aldehydes Nomenclature
Subscribe to RSS - Hemiacetal

Need Help?

We hope your visit has been a productive one. If you're having any problems, or would like to give some feedback, we'd love to hear from you.

For general help, questions, and suggestions, try our dedicated support forums.

If you need to contact the Course-Notes.Org web experience team, please use our contact form.

Need Notes?

While we strive to provide the most comprehensive notes for as many high school textbooks as possible, there are certainly going to be some that we miss. Drop us a note and let us know which textbooks you need. Be sure to include which edition of the textbook you are using! If we see enough demand, we'll do whatever we can to get those notes up on the site for you!