Discussions and Replies Session 3

ABSTRAK   Efendi, Syaiful. 2016. Perbedaan Kompetensi Produktif antara Siswa Kelas Industri dengan Kelas Reguler Paket Keahlian Teknik Kendaraan Ringan di SMKN 10 Malang. Skripsi, Jurusan Teknik Mesin, Fakultas Teknik, Universitas Negeri Malang. Pembimbing: (I) Dr. Syarif Suhartadi, M.Pd., (II) Drs. H. Agus Sholah, M.Pd. Kata Kunci: kompetensi produktif, kelas industri, kelas reguler   Tujuan SMK adalah menyiapkan siswa untuk memasuki lapangan kerja dan  mengembangkan sikap profesionalis. Hal ini dapat diwujudkan melalui kerjasama internal dengan membuka kelas kerjasama atau kelas industri pada SMK. SMKN 10 Malang adalah salah satu sekolah yang menerapkan kelas kerjasama dengan pihak Honda di jurusan teknik kendaraan ringan. Kelas tersebut bernama kelas HTEC (Honda Technician Education Class) yang dirilis sejak tanggal 10 Desember 2014. Tujuan dengan adanya kelas HTEC ini mampu meningkatkan kompetensi produktif siswa pada kelas XII agar  mempunyai kompetensi yang baik. Penelitian ini bertujuan untuk mengetahui perbedaan kompetensi produktif antara siswa kelas industri dengan kelas reguler. Desain penelitian ini termasuk dalam desain eksperimen dengan post-test only control design. Variabel dalam penelitian ini terdiri dari variabel bebas dan variabel terikat. Variabel bebas dalam penelitian ini adalah pengelompokkan kelas yang terdiri dari kelas industri dan kelas reguler sedangkan kompetensi produktif merupakan variabel terikat. Subyek penelitian ini adalah siswa kelas XII Teknik Kendaraan Ringan pada kelas industri dan kelas reguler menggunakancluster sampling dan proportional sample sebagai teknik pengambilan sampel penelitian. Teknik analisis data yang digunakan adalah teknik uji t (Independent Sample t-Test). Rata-rata nilai post-test kompetensi produktif siswa kelas industri adalah 83.8 dan rata-rata nilai post-test kompetensi produktif siswa kelas reguler adalah 76.94. Hasil uji t diperoleh nilai sig. (2 tailed

Why a feminist ethics of care and socio-ecological justice lens matter for global, interdisciplinary research on water security

In this conceptual analysis, we set out some of the negotiations and tensions that emerge when we try to build a shared understanding of water (in)security through the dual lenses of a feminist ethics of care and socio-ecological justice. We further reflect on how these theoretical lenses shape our work in practice—how do we actualise them in an international, interdisciplinary partnership? We actively seek to engage all our colleagues in how we understand the function of power and inequality in relation to the distribution of water resources and the ways in which intersectional inequalities shape access to, and availability of, water. We conclude that our international partnership will only add value to our understanding of water (in)security if we are able to identify not just how intersectional inequalities circumscribe differential access to water itself in a range of diverse contexts, but the ways socio-ecological justice and a feminist ethics of care are understood and in turn shape how we work together to achieve greater water security across diverse contexts

Photoreductive Changes of Phenyl-Selenium Bonds of Phenylselenoalkanes

Photo-induced-electron transfer from triethylamine to phenylselenoalkanes can lead to selective reduction and cleavage of the Ph-Se bond lending to the formation of benzene and the corresponding alkylselenyl radicals that dimerize

Painted Plaster

Home Page: Welcome to the online publication of the Villa Magna Project (2006–10). Our work involved the excavation and survey of a large imperial Roman villa and its estate, known from the letters of Marcus Aurelius, and the subsequent life of the site—its fortification in late antiquity, and the creation of a monastery among the ruins in the 10th century. The project was sponsored by the University of Pennsylvania’s Museum of Archaeology and Anthropology (Mediterranean Section), the British School at Rome, and the Soprintendenza ai Beni Archeologici del Lazio, with core funding from the 1984 Foundation, the Comune of Anagni and the BancAnagni Credito Cooperativo. This website includes the stratigraphic reports, object catalogues, physical anthropology, and environmental analyses for excavations at the site of Villa Magna, Italy. These materials are designed as a digital companion to the print volume Villa Magna: an Imperial Estate and its Legacies. Excavations 2006–2010. Use the headings above to explore the stratigraphy and finds from five years of excavation at the site, to view the data, or to learn more about the project itself

Synthesis of α-D-(1→3) and α-D-(1→4)-C-linked galactosides of D-mannose derivatives. Conformation of α-C-galactosides

Reductive radical alpha-D-galactosidation of 5-exo-(benzeneselenyl)-6-endo-chloro-3-methylidene-7- -oxabicyclo[2.2.1]heptan-2-one with acetobromo-D-galactose, followed by ketone reduction led to (+)-(1R,2S, 3R,4S,5S,6S)-5-exo-(benzeneselenyl)-6-endo-chloro-3-endo-[(2',3',4',6'-t etra-O-acetyl-alpha-D-galactopyranosyl)me- thyl]-7-oxabicyclo[2.2.1]heptan-2-endo-ol which was converted into (+)-methyl 3-deoxy-3-[(alpha-D-galactopyranosyl)methyl]-alpha-D-mannopyranoside (1), (+)-3-deoxy-3-[alpha-D-galactopyranosyl)methyl]-D-mannitol (2) and 4-deoxy-4-[(2',3',4',6'-tetra-O-acetyl-alpha-D-galactopyranosyl)methyl]- 2,3,6-tri-O-acetyl-D-mannono-1,5-lactone (3). H-1-MNR data of the alpha-C-galactosides confirmed that their preferred conformations involve antiperiplanar arrangements for the C-linked substrates and bond sigma C(1'),C(2') of the alpha-(1-->3)-C-galactoside unit. The alpha-(1-->3)-C-galactoside of methyl mannopyranoside 1 adopts a conformation similar to that proposed for methyl 3-O-(alpha-D-galactopyranosyl)-alpha-D-mannopyranoside

Synthesis of an Alpha-C-Galactoside of a Carbasugar - a New Class of Disaccharide Mimics

(+)-(1S,2S,3R,4R,5R)-2-[(2',3',4',6'-tetra-O-acetyl-alpha-D-galactopyran osyl)methyl]-5-methoxycyclohexa-1,3,4-triyl triacetate was derived from D-galactose and (1R,4R)-7-oxabicyclo[2.2.1]hept-5-en-2-one

Stereoselective synthesis of alpha-C-galactopyranosides of conduritols and aminoconduritols

Giese's radical glycosidation of (-)-(1S,4R,5R,6R)-5-exo-(benzeneselenyl)-6-endo-chloro-3-methylidene-7-o xabicyclo[2.2.1]-heptan-2-one with tetra-O-acetylbromo-alpha-D-galactopyranose gave a C-galactoside that was converted into (+)-(1S,2R,3S,4R)-6-chloro-3,3-endo-[(2',3',4',6'-tetra-O-acetyl-alpha-D -galactopyranosyl)methyl]-7-oxa-bicyclo[2.2.1]hept-5-en-2-endo-yl acetate ((+)-6). Treatment of (+)-6 with HBr, then with LiN3 and subsequent reduction afforded (3S,4R,5R,6S)-3-amino-1-chloro-4-[(alpha-D-galactopyranosyl)methyl]-cycl ohex-1-en-5,6-diol ((+)-10). Acidic hydrolysis of (+)-6 provided the (3R,4R,5R,6S)-1-chloro-4-[(alpha-D-galactopyranosyl)methyl]-cyclohex-hex -1-en-3,5,6-triol derivative (+)-11 or the (4R,5R,6S)-4-[(alpha-D-galactopyranosyl)methyl]-5,6-dihydroxycyclohex-2- en-1-one derivative (-)-12 selectively