Chemistry Synthesis Reaction Calculator?
Organic Synthesis Reaction Calculator?
Organic chemistry: “R and S naming”
Organic chemistry: “”. How to make and alkyl (). Reactions of and alkyl (with solvents, and , and ). Synthesis problems—using radical , E2, SN2, oxidation (PCC), and for synthesis. The “” technique for solving synthesis problems.
Organic chemistry: “More on and ”. attack on and ; the three main categories of attack. Two category 1 reactions: attack by a Grignard to form an alcohol; attack by LAH to form an alcohol. A category 2 reaction: attack by alcohol in acidic conditions to form an or . A category 2 “reverse” reaction: reaction of an or with aqueous acid to form an or
Organic chemistry: Three types of SN2 reaction
Organic chemistry: “Carboxylic acids and acid derivatives”. Acidity of carboxylic acids; ranking compounds in order of acidity. How to synthesize carboxylic acids: oxidation; carbonation; hydrolysis. The types of carboxylic acid derivative. The general pattern for attack on carboxylic acids and acid derivatives (addition-elimination). . Ranking carboxylic acids derivatives in order of reactivity
Organic chemistry: “ aromatic substitution”. aromatic substitution of benzene. Substitution through intermediates. Summary of methods for synthesis of phenols. oxidation to carboxylic acids; synthesis problems involving oxidation. Radical
Organic chemistry: “SN2, SN1, E2, and E1 reactions”
Organic chemistry: “ synthesis and reactions”. of carbons; acidity of alkynes; use of anions as for SN2 reactions and for attack on (). synthesis from by double elimination; synthesis from alkenes by -double . reactions. Hydrogenation of alkynes; hydrogenation of with catalyst to form alkenes; sequential one-electron reduction of alkynes with sodium metal to form trans alkenes. addition of HX to alkynes; addition of X2 to alkynes (). ; ; mercuric ion-catalyzed hydration of alkynes to form
Organic chemistry: “ of alkenes”. addition reactions. Addition of OsO4 (osmium ) to achieve . Using to achieve anti . A synthesis problem. The synthetic toolbox. When does hindrance block one face of a planar intermediate?
Organic chemistry: “More on SN2, SN1, E2, and E1 reactions”
Organic chemistry: “Radical reactions”.
Organic chemistry: “”. Addition reactions with alkenes: addition of H2 (hydrogenation); addition of HX (). vs. anti-.
Organic chemistry: “Retro Diels-Alder reaction”.
Organic chemistry: “Synthesis using addition to alkenes”. Some synthesis problems involving alkenes and addition.
Organic chemistry: “ reactions”.
Organic chemistry: “Synthetic strategies for substituted benzenes”. S
Organic Synthesis - Organic Chemistry Portal
Chemistry: “Electrochemistry and electrochemical cells”. Electrochemistry and electrochemical cells. Oxidation and reduction; oxidizing agents vs. reducing agents. Galvanic/voltaic cells. Cathode, anode. Free energy and cell potential. Half-reactions; reduction potentials, oxidation potentials. Salt bridge. Calculating cell potential. Faradays constant. Work. Equilibrium constant. Nernst equation. Electrolytic cells
Online organic chemistry synthesis solver: ..
Organic chemistry: “How to draw resonance structures”. The meaning of resonance. The purpose of resonance is to determine the locations of the charges. How to interpret electron-pushing arrows. Rules for drawing legal and significant resonance structures.
Program that simulates basic reactions in organic chemistry
Organic chemistry: “Electron-pushing arrows”. How to use electron-pushing arrows, also known as “curved arrows,” to draw intermediates and products in reaction mechanisms.
Reaction Prediction | Organic Chemistry Resources …
It is estimated that at least 25 percent of all chemical reactions in the pharmaceutical industry use the palladium-catalyzed cross coupling that earned Negishi the 2010 Nobel Prize in chemistry shared with Richard Heck and Akira Suzuki. His techniques to link carbon atoms together allow for easy and efficient synthesis of complex organic compounds used in everything from pharmaceuticals to electronics. In addition to the painkiller naproxen and the cancer treatment taxol, Negishi coupling has been used in fluorescent marking essential for DNA sequencing and in the creation of materials for thin LED displays.
Organic chemistry: “E2 reactions”. Introduction to the E2 mechanism. E2 stereochemistry-- vs. trans, determined by anti- transition state. vs. solvents. SN2 stereochemistry
Freelance Teacher - Physics Chemistry, Organic Chemistry
Organic chemistry: “Some SN2, SN1, E2, and E1 topics”. Polar vs. solvents. rearrangements. E2 and E1 ( vs. Hofmann). transition state for E2; E2 and
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