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H 2
H 2

... and type of both reactants and products.  In this section you will analyze common chemical reactions.  The goal is to give you the background information necessary to determine the type of product when given the reactants.  There are seven of these reactions. You have already had experience with ...
Stoichiometry - VernonScienceLSA
Stoichiometry - VernonScienceLSA

... amount is called the LIMITING REACTANT. Since the limiting reactant gets completely used up first, it sets the limit on the amount of product that can be formed and the amount of the excess reactant used in the reaction. LIMITING REACTANT is the reactant that sets a limit on the amount of product th ...
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Full answers
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... As the reaction is endothermic, the energy of the products is higher than that of the reactants. Would you expect the forward or the reverse reaction to be faster? Why? The backward reaction would be faster as it has a lower activation energy. This is a consequence of the reaction being endothermic. ...
Physical Setting/Chemistry Examination
Physical Setting/Chemistry Examination

... question on your separate answer sheet. Write your answers to the Part B–2 and Part C questions in your answer booklet. All work should be written in pen, except for graphs and drawings, which should be done in pencil. You may use scrap paper to work out the answers to the questions, but be sure to ...
Chem 171 Review - Exam 1
Chem 171 Review - Exam 1

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ΔG - Lemon Bay High School

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Qualitative Analysis Lab
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Catalyst Notes - University of Idaho
Catalyst Notes - University of Idaho

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... The gas-phase decomposition of dinitrogen monoxide is considered to occur in two steps. k1 Step 1: N2O(g)  N2(g) + O(g) k2 Step 2: N2O(g) + O(g)  N2(g) + O2(g) ...
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APPLICATION OF IONIC LIQUIDS IN ORGANIC SYNTHESIS

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Hydrolases as Catalysts for Green Chemistry and

... produced in a solvent-free reaction. Engineering the molar ratio of the substrates in the reaction and adding a step involving hydrolysis of the by-product resulted in final yield of 99 %. Comparison with earlier reports based on green metrics showed the method to have a greener profile. Another pro ...
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Process chemistry

Process chemistry is the arm of pharmaceutical chemistry concerned with the development and optimization of a synthetic scheme and pilot plant procedure to manufacture compounds for the drug development phase. Process chemistry is distinguished from medicinal chemistry, which is the arm of pharmaceutical chemistry tasked with designing and synthesizing molecules on small scale in the early drug discovery phase.Medicinal chemists are largely concerned with synthesizing a large number of compounds as quickly as possible from easily tunable chemical building blocks (usually for SAR studies). In general, the repertoire of reactions utilized in discovery chemistry is somewhat narrow (for example, the Buchwald-Hartwig amination, Suzuki coupling and reductive amination are commonplace reactions). In contrast, process chemists are tasked with identifying a chemical process that is safe, cost and labor efficient, “green,” and reproducible, among other considerations. Oftentimes, in searching for the shortest, most efficient synthetic route, process chemists must devise creative synthetic solutions that eliminate costly functional group manipulations and oxidation/reduction steps.This article will focus exclusively on the chemical and manufacturing processes associated with the production of small molecule drugs. Biological medical products (more commonly called “biologics”) represent a growing proportion of approved therapies, but the manufacturing processes of these products are beyond the scope of this article. Additionally, the many complex factors associated with chemical plant engineering (for example, heat transfer and reactor design) and drug formulation will be treated cursorily.
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