(a)
Interpretation: The lactol formed from intramolecular cyclization of given hydroxyl aldehyde is to be predicted.
Concept introduction:
Cyclic hemiacetals containing five or six-membered rings are generally stable and can be isolated.
(b)
Interpretation: The lactol formed from intramolecular cyclization of given hydroxyl aldehyde is to be predicted.
Concept introduction: Aldehydes or ketones on reaction with one equivalent of alcohol form hemiacetal and on reaction with two equivalents of alcohol it forms acetals. This is nucleophilic addition reaction. These reactions takes place in presence of acids, commonly
Cyclic hemiacetals containing five or six-membered rings are generally stable and can be isolated.
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Chapter 21 Solutions
Organic Chemistry
- Give the IUPAC name for each aldehyde.arrow_forwardDraw the products formed when each alkyl halide is treated with NaCN.arrow_forwardWhat enolate is formed when each ketone is treated with LDA in THF solution? What enolate is formed when these same ketones are treated with NaOCH3 in CH3OH solution?arrow_forward
- What alcohol starting material is needed to prepare each carbonyl compound as a product of an oxidation reaction?arrow_forwardWhat alkyl halides are formed when attached ether is treated with HBr?arrow_forwardDraw the product formed when phenylacetic acid (C6H5CH2COOH) is treated with each reagent. With some reagents, no reaction occurs. (A - F)arrow_forward
- Draw the product formed when CH3CH2CH2CH2NH2 reacts with each carbonyl compound in the presence of mild acidarrow_forwardDraw all stereoisomers formed when each alkene is treated with mCPBAarrow_forwardHow would you convert cyclohexanone into each compound using any required inorganic reagents and needed organic compounds? a. b.arrow_forward
- What is the product formed when each dicarbonyl compound undergoes an intramolecular aldol reaction, followed by dehydration.arrow_forwardWhat lactol (cyclic hemiacetal) is formed from intramolecular cyclization of each hydroxy aldehyde?arrow_forwardDraw two different ways to prepare each ketone from an acid chloride and an organocuprate reagent.arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning