1 2014-1435. Learning Objectives Chapter eight introduces carbonyl compounds and reactions that involve a nucleophilic attack at the carbonyl carbon in.

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Learning Objectives Chapter eight introduces carbonyl compounds and reactions that involve a nucleophilic attack at the carbonyl carbon in addition to the other topics. By the end of this chapter the student will:  Know the structural differences between aldehydes and ketones  Know how to draw aldehydes and ketones  know the common and IUPAC nomenclature of aldehydes and ketones  Know the physical properties of aldehydes and ketones  Know how to synthesize an aldehyde or a ketone from a compound without that functionality. functionality.  Know the different nucleophilic attack reactions at the carbonyl carbon and the specific products formed in each case. specific products formed in each case. King Saud University Chemistry Department

ALDEHYDES: STRUCTURE AND NOMENCLATURE  General formula: RCHO or  Bond line formula  The aldehyde group is always (terminal)at the end of a chain Chem. Common Nomenclature Of Aldehydes  Some aliphatic aldehydes have common names which have to be memorized. Formaldehyde Acetaldehyde Propionaldehyde Butyraldehyde King Saud University Chemistry Department

4  Some aromatic aldehydes have common names such as: Salicylaldehyde (o-Hydroxybenzaldehyde) Anisaldehyde (p-methoxybezaldehyde) IUPAC Nomenclature to get the name of the parent hydrocarbon, then replace the ending e by the suffix –al  Select the longest continuous carbon chain that contains the H-C=O group to get the name of the parent hydrocarbon, then replace the ending e by the suffix –al such as C=O(ketone),–OH, C=C, CΞC, OR  The CHO group is assigned the locant 1 and takes precedence over other functional groups that may present such as such as C=O(ketone),–OH, C=C, CΞC, OR King Saud University Chemistry Department

5 Methanal Ethanal Propanal Butanal 3-Chlorobutanal 3-Hyydroxypropanal 2-Butenal Cyclohexencarbaldehyde  Aromatic aldehydes are usually designated as derivatives of the simplest aromatic aldehyde, Benzaldehyde. Benzaldehyde 4-Nitrobenzaldehyde 2-Hydroxybenzaldehyde 4- Methoxybenzaldehyde King Saud University Chemistry Department

 General formula: RCOR’ (R and R’=alkyl or aryl) derived by listing the alkyl  Common names of ketones derived by listing the alkyl substituents attached to the carbonyl group in alphabetical order, followed by the word ketone. 6 KETONES:STRUCTUR AND NOMENCLATURE KETONES:STRUCTUR AND NOMENCLATURE Acetone Acetophenone Benzophenone Dimethyl ketone Methyl phenyl ketone Methyl vinyl ketone Diphenyl ketone King Saud University Chemistry Department

IUPAC Nomencalture : to get the name of the parent hydrocarbon, then replace the ending e by the suffix –one  Select the longest continuous carbon chain that contains the C=O group to get the name of the parent hydrocarbon, then replace the ending e by the suffix –one  The chain is numbered in such a way as give the lowest number to the C=O group. 7 King Saud University Chemistry Department

Propanone Phenyl ethanone 3-Buten-2-one Diphenylmethanone Cyclopentylpropanone 3-Ethyl-2-hydroxycyclohexanone 5-Oxohexanal King Saud University Chemistry Department

Physical Properties OF Aldehydes And Ketones  Because the polarity of the carbonyl group, aldehydes and ketones are polar compounds. A-Boiling and melting points  Higher melting and boiling points compared to analogous alkanes due to they show dipole- dipole attractions.  These attractions although important, are not as strong as interactions due to hydrogen bonding as a result, the boiling points of aldehydes and ketones are higher than those of non polar alkanes, but lower than those of alcohols whose molecules are connected together by H-bonds. B-Solubility  Lower aldehydes and ketones are are more soluble than alkanes but less soluble than alcohols in aqueous media King Saud University Chemistry Department

Preparation Of Aldehydes And ketones 1- Oxidation of Alcohols 2- Ozonolysis of Alkenes; results in formation of aldehydes or ketones depending on structure of the alkene used. King Saud University Chemistry Department

3- Hydration Of Alkynes 4- Friedel Crafts Acylation N.B: -COR group is m-director and deactivating towards electrophiles King Saud University Chemistry Department

Reactions Of Aldehydes And Ketones (Nucleophilic addition reactions) 1- Reduction : Formation Of Alcohols King Saud University Chemistry Department

2-Nucleophilic addition of Grignard reagent (formation of alcohols)  Addition of RMgX to formaldehyde gives 1 ◦ alc.  Addition of RMgX to any other aldehyde gives 2 ◦ alc.  Addition of RMgX to ketones gives 3 ◦ alc. 3- Oxidation reaction Only aldehydes can be oxidized ketones resist oxidation King Saud University Chemistry Department

5-Addition of Hydrogen Cyanide: Formation Of Cynohydrins King Saud University Chemistry Department

6- Addition Of Alcohols: King Saud University Chemistry Department

16 7- Addition of Ammonia and Ammonia Derivatives 145 Chem. King Saud University Chemistry Department

Exercises 1- The correct name of the following compound is: A) 3-hydroxyhexanal B) 3-hydroxy-4-hexenal C) 4-hydroxy-5-hexenal D)3-hydroxy-1-hexenal 2- The structure of Acetal is: 145 Chem. 17 King Saud University Chemistry Department

145 Chem Reaction of phenyhydrazine with carbonyl compounds (aldyhydes or ketones) gives: A) OximeB) PhenylhydrazoneC) ImineD) Hemiacetal 4 - Which of the following compounds has the highest boiling point? King Saud University Chemistry Department

Questions?