Conversion to Cyclic Acetals

Description

22.5 E
Danielle Thibeadeaux
Flashcards by Danielle Thibeadeaux, updated more than 1 year ago
Danielle Thibeadeaux
Created by Danielle Thibeadeaux over 10 years ago
26
0

Resource summary

Question Answer
Aldehydes and ketones react with open- chain __ , __ _____ to produce ______ _______. Aldehydes and ketones react with open-chain 1,2 diols to produce cyclic acetals.
If the 1, 2 diol is attached to a ring as in a monosaccharide, formation of the cyclic acetals occurs only _________________________________________________________. If the 1,2 diol is attached to a ring as in a monosaccharide, formation of the cyclic acetals occurs only when the vicinal(any two functional groups bonded to two adjacent atoms) hydroxyl groups are cis to each other.
Cyclic acetals are commonly used to protect ________ ____ hydroxyl groups of a sugar while reactions are carried out on other parts of the molecule. Cyclic acetals are commonly used to protect vicinal cis hydroxyl groups of a sugar while reactions are carried out on other parts of the molecule.
When acetals are formed from acetone they are called acetonides. What are acetonides? In organic chemistry, an acetonide is the functional group composed of the ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. It is the most common protecting group for 1,2- and 1,3-diols. The protecting group can be removed by hydrolysis of the ketal using dilute aqueous acid.
Show full summary Hide full summary

Similar

A Level Chemistry Unit 1 - Organic Chemistry
charlottehyde
Water and Organic Macromolecules
Selam H
Organic Chemistry
Ella Wolf
A2 Organic Chemistry - Reactions
yannycollins
C2: Material Choices Test
James McConnell
CARBOHYDRATES & SUGARS
Eleanor H
Crude Oils and others quiz
Dale George
Organic Nomenclature
mahnoor.gohar
Carbohydrates
kevinlinkovoor
Alcohols
Bee Brittain
Polymerisation.
anjumn10