{"id":22358,"date":"2020-05-02T23:26:26","date_gmt":"2020-05-02T23:26:26","guid":{"rendered":"https:\/\/www.sohag-univ.edu.eg\/facsci\/?p=22358"},"modified":"2020-05-02T23:26:26","modified_gmt":"2020-05-02T23:26:26","slug":"%d8%a7%d9%84%d8%ab%d8%a7%d9%84%d8%ab%d8%a9-%d9%83%d9%8a%d9%85%d9%8a%d8%a7%d8%a1-%d9%88%d9%85%d9%8a%d9%83%d8%b1%d9%88%d8%a8%d9%8a%d9%88%d9%84%d9%88%d8%ac%d9%8a-%d9%83%d9%8a%d9%85%d9%8a%d8%a7%d8%a1","status":"publish","type":"post","link":"https:\/\/sci.sohag-univ.edu.eg\/main\/%d8%a7%d9%84%d8%ab%d8%a7%d9%84%d8%ab%d8%a9-%d9%83%d9%8a%d9%85%d9%8a%d8%a7%d8%a1-%d9%88%d9%85%d9%8a%d9%83%d8%b1%d9%88%d8%a8%d9%8a%d9%88%d9%84%d9%88%d8%ac%d9%8a-%d9%83%d9%8a%d9%85%d9%8a%d8%a7%d8%a1\/","title":{"rendered":"\u0627\u0644\u062b\u0627\u0644\u062b\u0629  \u0643\u064a\u0645\u064a\u0627\u0621 \u0648\u0645\u064a\u0643\u0631\u0648\u0628\u064a\u0648\u0644\u0648\u062c\u064a \u0643\u064a\u0645\u064a\u0627\u0621 \u0648\u062d\u064a\u0648\u0627\u0646 \u0643\u064a\u0645\u064a\u0627\u0621 \u0648\u0646\u0628\u0627\u062a \u0643\u064a\u0645\u064a\u0627\u0621 \u0648\u0641\u064a\u0632\u064a\u0627\u0621  \u0643\u064a\u0645\u064a\u0627\u0621 \u0648\u062c\u0648\u0644\u0648\u062c\u064a\u0627 \u0643\u064a\u0645\u064a\u0627\u0621 \u0639\u0636\u0648\u064a\u0629 364\u0643 \u0623.\u062f. \u0646\u062c\u0648\u064a \u0627\u0644\u0635\u0627\u0648\u064a \u062f.\u0627\u064a\u0645\u0627\u0646 \u0639\u0628\u062f \u0627\u0644\u0644\u0647 \u062f.\u0639\u0628\u062f \u0627\u0644\u0631\u062d\u064a\u0645 \u0645\u062d\u0645\u062f"},"content":{"rendered":"<p dir=\"ltr\" style=\"text-align: center;\"><strong>Model 1<\/strong><\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(A)\u00a0\u00a0\u00a0 Ketone bodies and ketolysis<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(B)\u00a0\u00a0\u00a0 Isolated systems in polynuclear hydrocarbons (synthesis and properties of three examples).<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(C)\u00a0\u00a0\u00a0 Electrophilic aromatic substitution in pyridine and pyrrole.<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(D)\u00a0\u00a0\u00a0 Oxidation- reduction reactions of monosaccharides (aldoses and ketosis)<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\"><strong>Model 2<\/strong><\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(A)\u00a0\u00a0\u00a0 Diabetes mellitus<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(B)\u00a0\u00a0\u00a0 Naphthalene (structure and synthesis).<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(C)\u00a0\u00a0\u00a0 Electrophilic and nucleophilic aromatic substitution in pyridine.<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">\u00a0 \u00a0 \u00a0 \u00a0(D) Cyclic structure of monosaccharide.<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\"><strong>Model 3<\/strong><\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(A)\u00a0\u00a0\u00a0\u00a0 Variations in normal blood glucose<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(B)\u00a0\u00a0\u00a0\u00a0 Naphthols (synthesis and properties of 1- and 2-naphthol).<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(C)\u00a0\u00a0\u00a0\u00a0 Similarities and differencies between pyrrole and furan (reactions, reactivity)<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(D)\u00a0\u00a0\u00a0\u00a0 Reactions of monosaccharide (glucose).<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">\n<p dir=\"ltr\" style=\"text-align: center;\"><strong>Model 4<\/strong><\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(A)\u00a0\u00a0\u00a0\u00a0 Gluconeogenesis<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(B)\u00a0\u00a0\u00a0\u00a0 Substitution reactions of naphthalene.<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(C)\u00a0\u00a0\u00a0\u00a0 Basic properties of pyrrole and pyridine<\/p>\n<p dir=\"ltr\" style=\"text-align: center;\">(D)\u00a0 \u00a0 \u00a0Disaccharides<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Model 1 (A)\u00a0\u00a0\u00a0 Ketone bodies and ketolysis (B)\u00a0\u00a0\u00a0 Isolated systems in polynuclear hydrocarbons (synthesis and properties of three examples). (C)\u00a0\u00a0\u00a0 Electrophilic aromatic substitution in pyridine and pyrrole. (D)\u00a0\u00a0\u00a0 Oxidation- reduction reactions of monosaccharides (aldoses and ketosis) Model 2 (A)\u00a0\u00a0\u00a0 Diabetes mellitus (B)\u00a0\u00a0\u00a0 Naphthalene (structure and synthesis). (C)\u00a0\u00a0\u00a0 Electrophilic and nucleophilic aromatic substitution in pyridine. \u00a0 [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"zakra_page_container_layout":"customizer","zakra_page_sidebar_layout":"customizer","zakra_remove_content_margin":false,"zakra_sidebar":"customizer","zakra_transparent_header":"customizer","zakra_logo":0,"zakra_main_header_style":"default","zakra_menu_item_color":"","zakra_menu_item_hover_color":"","zakra_menu_item_active_color":"","zakra_menu_active_style":"","zakra_page_header":true,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-22358","post","type-post","status-publish","format-standard","hentry","category-1"],"rttpg_featured_image_url":null,"rttpg_author":{"display_name":"admin","author_link":"https:\/\/sci.sohag-univ.edu.eg\/main\/author\/admin\/"},"rttpg_comment":1,"rttpg_category":"<a href=\"https:\/\/sci.sohag-univ.edu.eg\/main\/category\/%d8%a7%d8%ae%d8%a8%d8%a7%d8%b1-%d9%82%d8%b3%d9%85-%d8%a7%d9%84%d9%81%d9%8a%d8%b2%d9%8a%d8%a7%d8%a1\/\" rel=\"category tag\">\u0627\u062e\u0628\u0627\u0631 \u0642\u0633\u0645 \u0627\u0644\u0641\u064a\u0632\u064a\u0627\u0621<\/a>","rttpg_excerpt":"Model 1 (A)\u00a0\u00a0\u00a0 Ketone bodies and ketolysis (B)\u00a0\u00a0\u00a0 Isolated systems in polynuclear hydrocarbons (synthesis and properties of three examples). (C)\u00a0\u00a0\u00a0 Electrophilic aromatic substitution in pyridine and pyrrole. (D)\u00a0\u00a0\u00a0 Oxidation- reduction reactions of monosaccharides (aldoses and ketosis) Model 2 (A)\u00a0\u00a0\u00a0 Diabetes mellitus (B)\u00a0\u00a0\u00a0 Naphthalene (structure and synthesis). (C)\u00a0\u00a0\u00a0 Electrophilic and nucleophilic aromatic substitution in pyridine. \u00a0&hellip;","_links":{"self":[{"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/posts\/22358","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/comments?post=22358"}],"version-history":[{"count":1,"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/posts\/22358\/revisions"}],"predecessor-version":[{"id":22359,"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/posts\/22358\/revisions\/22359"}],"wp:attachment":[{"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/media?parent=22358"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/categories?post=22358"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/sci.sohag-univ.edu.eg\/main\/wp-json\/wp\/v2\/tags?post=22358"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}