1 1-Nonanol 2- Nonenal

Nonachloro-5,5-dihydrox3q)enta-cyclo[5.3.0.0 .0 .0 ]decane, see Kepone Nonanal, see Nonane Nonanoic acid, see Nonane 1-Nonanol, see Nonane 1-Nonene, see Nonane Nonyl hydroperoxide, see Nonane Norchloralachlor, see Alachlor Octachlorobiphenyl, see Pentachlorobenzene Octachlorocyclopentene, see Hexachlorobutadiene Octachlorodibenzo-/>dioxin, see Pentachlorophenol Octachlorodiphenylene dioxide, see Pentachlorophenol l,2,3,4,4a,9,10,10a-0ctahydrophenanthrene, see Phenanthrene... 

Di-N-Butyl Ketone Nonene 1-Nonene Nonene Nonanol... 

Nonanol 1-Nonene Nonyl mercaptan 1-Nonyne Octadecane Octanal Octane Octanoic acid... 

More recently, the total volatile composition of distilled cucumbers was investigated by a number of groups (2, ). The steam volatile con unds of muskmelons fCucumis melo) have also received attention (, , 6,) as have those of watermelons (Citrullus vulgaris) (7.) The most striking feature in the volatile con onents of all these fruits is the variety and magnitude of the nine-carbon compounds. These compounds include nonanol, nonanal, various nonenols, nonadienols, nonenals and nonadienals. 

Figure 4. Testosterone concentration (ng/ml) in temporal gland secretion and relative abundance of four groups (I-IV) of compounds present in TGS over the course of musth in Tunga, an Asian bull elephant (a different elephant from the previous figures). Group I cyclohexanone, benzoic acid, phenylacetic acid, phenylpropanoic acid, octanoic acid, 3-octen-2-one and4-n-nonylphenol. Group II 5-nonanol, 2-hydroxyacetophenone, 1,3 dihydro-2H-indol-2-one, 2-nonanone, unidentified and 3-nonen-2-one. Group III phenol, decanoic acid and famesol. Group IV 4-hexenoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic acid and dotriacontanol.

Nonanal 1,3-Nonanediol acetate, mixed esters Nonanoic acid 2-Nonanol 2-Nonanone 3-Nonanon-1-yl acetate trans-2-Nonenal cis-6-Nonen-1-ol trans-2-Nonen-1-ol n-Nonyl acetate... 

Dehydration of 2-methyl-2-spiro[4.4]nonanol gives a mixture containing l-methyl-6-bicyclo[4.3.0]nonene. Write a mechanism that accounts for the formation of this product. 

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