Journal of Chemical Education. Oct92, Vol. 69 Issue 10, p779. 4p. 12 Diagrams.
Subjects
CHEMISTRY education in universities & colleges and ORGANIC chemistry
Abstract
Discusses a modern approach to teaching organic chemistry. Organic chemistry courses must begin with structure. Suggests using nuclear magnetic resonance spectroscopy to introduce structure; Introduce students to symmetry axes and planes; Review valence of hydrogen and first-row elements; Give them the equation for calculating the number of sites of unsaturation from the molecular formula; Give students the results of 13C{1H} DEPT with details later; More.
Examines proposed partial least squares (PLS) multivariate statistical models for predicting concentration of hydrocarbon- and oxygen-containing functional groups for a calibration set of model homopolymers. Plasma-deposited films; Static secondary ion mass spectrometry (SIMS); PLS modeling; Preprocessing; Prediction of surface oxygen and hydrogen concentration.
SEDIMENTATION & deposition research, OCEAN bottom, and CARBONATE minerals
Abstract
Discusses the mechanism underlying the relative deposition rates of organic carbon and calcite to the sea floor. Effect of total calcite concentration on the specific depth at which calcite dissolves; Control of atmospheric carbon dioxide by ocean carbonate chemistry; Organic carbon degradation in the sediments.
GUMS & resins, ALLERGIES, COLOPHONS, GLYCERYL ethers, PATIENTS, and NUCLEAR magnetic resonance
Abstract
In the esterification of rosin with glycerol, the main compound formed, glyceryl triabietate, shows low allergenic activity. In this study, compounds formed in smaller amounts, when abietic add (main component in rosin) was esterified with glycerol, were identified as glyceryl-1-monoabietate (GMA), glyceryl-1,2-diabietate (GDA,1,2) and glycery-1,3-diabietate (GDA1,3), using nuclear magnetic resonance (NMR), infra-red (IR) and mass spectrometry (MS) analyses. According to animal experiments, OMA was a contact allergen. No cross-reactivity was seen to allergens in unmodified rosin. Some patients allergic to unmodified rosin reacted when tested with GMA. No reactions were seen to the 2 diabietates. Some patients also reacted to commercial glycerol-modified rosins. OMA together with unmodified abietic acid were identified in these rosin samples. The reactions seen in rosin-sensitive patients to commercial glycerol-esterified rosins probably derive from the unmodified material still present in the product, but could also be the result of OMA obtained from the glycerol derivatization. [ABSTRACT FROM AUTHOR]
INSECT sex attractants, GRACILLARIIDAE, TORTRICIDAE, YPONOMEUTIDAE, OECOPHORIDAE, PYRALIDAE, GELECHIIDAE, and ALCOHOLS (Chemical class)
Abstract
Field screening tests of 21 saturated and monounsaturated straight chain C12 and C14 alcohols and their acetates as well as some binary mixtures in dosages of 1 and 0.2 mg/dispenser were carried out in Lithuanian in 1993 and 1994. New sex attractants were determined for males of five moth species of the family Gracillariidae ( E10-12:OH for Phyllonorycter sorbi, E10-12Ac for Ph. cydoniella and Ph. oxyacanthae, Z10-12:OAc for Ph. junoniella, and a mixture of Z10-14:OAc with E9-14:OAc in a 1:10 for Ph. sylvella), for four species of the family Tortricidae ( E10-14:OAc for Endothenia ericetana, Z10-14:OAc in a 10:1 mixture with E11-14:OAc for Eudemis pozphyrana, E11-14:OAc in a 10:1 mixture with E11-14:OH for Dichrorampha petiverella and Cochylis dubitana), for two species of Gelechiidae ( Z9-14:OAc in a mixture with either Z10-14:OAc in a ratio 1:1, E9-14:OAc in a ratio 1:10 or E10-14:OAc in a ratio 10:1 for Bryotropha galhanella, Z10-14:OAc and E9-14:OAc in a ratio 10:1 for B. mundella), as well as for one species of each of the families Yponomeutidae ( Z7-14:OAc for Paraswammerdamia lutarea) and Oecophoridae ( Z10-14:OAc and E9-14:OAc in a ratio 10:1 for Pseudatemelia josephinae). Preliminary composition of sex attractants was established for three moth species of the family Gracillariidae ( Z10-14:OAc in a 1:10 mixture with E9-14:OAc for Phyllonorycter heegerella, Ph. coryli and Ph. dubitella) and for one species of the family Gelechiidae ( Z9-14:OAc for Bryotropha terella). Inhibitors of the sex attractants were found for four leafminer species of the family Gracillariidae ( Z7-, Z9- and Z10-12:OAc for Phyllonorycter sorbi, Z10-, E10-12:OH and E10-14:OH for Ph. mespilella, E10-12:OH for Ph. cydoniella, Z10-12:OH and E10-14:OH for Ph. oxyacanthae), for three species of Tortricidae ( E9-, Z11- and E11-14:OAc for Endothenia ericetana, E11-14:OAc for Gypsonoma minutana, E10- and E11-14:OAc for Epagoge grotiana), and for one species from the family Pyralidae ( Z10-, E10- and E11-14:OAc for Pyrausta aurata). Data from male behaviour tests in tube olfactometers are presented for Phyllonorycter blancardella, Ph. sorbi, Ph. dubitella and Ph. strigulatella and active compounds revealed. [ABSTRACT FROM AUTHOR]
LEAFMINERS, INSECT sex attractants, and PHEROMONES
Abstract
Dodecyl acetate (12:OAc) (E)-10-dodecenyl acetate (E10-12:OAc) and (E)-10-dodecenol (E10-12:OH) in the ratio 8 : 80 : 12 were collected by solid phase micro-extraction of the volatiles emitted by virgin signalling females of the spotted tentiform leafminer moth, Phyllonorycter blancardella. The same compounds in the ratio 8 : 79 : 13 were extracted from the sex pheromone glands of virgin signalling females of the same species. The chemical structures of the compounds were identified by gas chromatography and mass spectrometry. Trapping results obtained from field tests using synthetic components of the sex pheromone demonstrated that only one component, E10–12:OAc, was essential for the attraction of conspecific males and should be considered as a sex pheromone. [ABSTRACT FROM AUTHOR]
THERMAL analysis, THERMODYNAMICS, INORGANIC chemistry, ORGANIC compounds, and POLYMERS
Abstract
Summarizes developments and applications in thermal analysis that appeared in Chemical Abstracts from October 1997 to October 1999. Instrumentation; Thermodynamic measurements; Kinetic considerations; Inorganic chemistry; Organic and polymeric materials; Biochemical and natural products; Pharmaceutical applications; Minerals.
OLFACTORY nerve, TOBACCO, MOTH flies, SMELL, CHROMATOGRAPHIC analysis, and ELECTROPHYSIOLOGY
Abstract
An important question in olfaction is for which odorants receptor neurones have evolved. In the present study, olfactory receptor neurones on the antennae of the tobacco budworm moth Heliothis virescens were screened for sensitivity to naturally occurring plant-produced volatiles by the use of gas chromatography linked to electrophysiology. Volatiles of host as well as non-host plants collected by headspace techniques were used for stimulating the neurones, sequentially via two columns, one polar and one nonpolar installed in parallel in the gas chromatograph. Three types of neurones presented in this paper responded to one, two or three compounds for which the retention times were determined in both column types. The chemical structures of the active components were determined on the basis of mass spectrometry linked to gas chromatography, indicating E-β-ocimene and β-myrcene as stimulants for neurone type 1, E,E-α-farnesene for neurone type 2 and homo-farnesene for neurone type 3. Re-testing authentic materials verified the identifications for the type 1 neurones. The results demonstrate a high specificity for the three types of neurones by strong responses to one or two structurally similar compounds out of hundreds present in a large variety of plants. The study exemplifies plant odour detection by narrowly tuned receptor neurones in a polyphagous moth species. [ABSTRACT FROM AUTHOR]