SSL Themes in the Gospel of John Q424

Institution Seventh Day Adventist Church Adult Lesson
Course SDA CHURCH
Year 1st Year
Semester Unknown
Posted By stephen oyake rabilo
File Type pdf
Pages 176 Pages
File Size 6.2 MB
Views 2878
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Description

Sitting in a shop in Tehran, Iran, the Persian rug depicted an ancient forest. Beautifully done, it re-created a scene in Switzerland: mountains, a waterfalls, a turquoise lake, forested hillsides, and an expansive blue sky dotted with clouds. Anyone in that shop could have spent their time noting the details: the number of knots per square inch, the fabric of the carpet, the types of dye used—all the minutiae that resulted in the rug. Or the person could have focused, instead, on the arresting techniques and themes that gave the carpet its unique beauty: the sky reflected in the lake, the snow that capped the mountains, the verdant forest complemented by the deep green moss. The themes of the carpet combined with one another in a deftly coordinated display of beauty to manifest the splendor of that serene spot in the Alps. This quarter we will be studying another finely crafted masterpiece. This work is not the result of a brush on canvas, or a precisely framed photograph, or a skillfully woven carpet. Rather, it is the Word of God, as artfully expressed in the Gospel of John. Words have meaning within their contexts. For anyone to understand what Scripture intends to say, it must be studied in context—the immediate sentences, chapters, and sections, and the overall message of the Bible itself. Finally, because the entire Bible is inspired by the Holy Spirit, each part should be studied in the context of the whole.
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Reactions of Alkyl halides
In this type of reaction, a nucleophile reacts with haloalkane (the substrate) having a partial positive charge on the carbon atom bonded to halogen. A substitution reaction takes place and halogen atom, called leaving group departs as halide ion. Since the substitution reaction is initiated by a nucleophile, it is called nucleophilic substitution reaction
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Substitution and Elimination Electron Flow Pathway
Path Limitations There are three requirements for the S N 2 reaction. In order to be pushed out, the leaving group must be at least fair, usually good. The nucleophile also must be reactive enough to push out the leaving group. Finally, the back side of the tetrahedral carbon attacked must be accessible to the nucleophile and not blocked by other groups.
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The SN2 reaction
The hydroxide ion is a good nucleophile since the oxygen atom has a negative charge and a pair of unshared electrons. The carbon atom is electrophilic since it is bound to a (more electronegative) halogen, which pulls electron density away from the carbon, thus polarizing the bond with carbon bearing partial positive charge and the halogen bearing partial negative charge. The nucleophile is attracted to the electrophile by electrostatic charges. The nucleophile attacks the electrophilic carbon through donation of 2 electrons. Carbon can only have a maximum of 8 valence electrons, so as the carbon nucleophile bond is forming, then the carbon-leaving group bond must be breaking. Iodide is the leaving group since it leaves with the pair of electrons that once bound it to carbon.
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