Ochem 2 practice synthesis problems

    • [PDF File]Undergraduate Organic Synthesis Guide

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      synthesis problems. You will bomb a fill-in-the-blank synthesis question if you don’t know your reactions cold. This handout is nowhere near exhaustive—study the lecture notes too. 2) Look at the Point Value of the Problem In general, more points are assigned to synthesis problems that have longer routes involving more reactions.

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    • [PDF File]COMMON SYNTHETIC SEQUENCES FOR OCHEM I

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      A synthesis is a series of two or more reactions designed to obtain a specific final product. A synthetic step ... COMMON SYNTHETIC SEQUENCES FOR OCHEM I. 1. STARTING WITH AN ALKANE, PROVIDE A SYNTHESIS FOR A MOLECULE THAT HAS A ... First question to ask in a lot of synthetic problems is, given the functional group I’m supposed to prepare, ...

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    • [PDF File]Multistep Organic Synthesis - University of Manitoba

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      Multistep Organic Synthesis ... There are a few simple practice problems at the end of Chapter 12 that are worth doing, and you will also find other problems in the various reaction chapters that ask you to “propose a synthesis”.

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    • [PDF File]Organic Chemistry 32-235 Practice Questions for Exam #2 ONE

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      Organic Chemistry 32-235 Practice Questions for Exam #2 Part 1: (Circle only ONE choice, circling more than one will be counted as wrong!) 4 points each 1. The …

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    • Multi-step Organic Synthesis

      Example #2: Synthesis of indynaprost from cyclopentadiene into O H H HO HO HO 2C ... for chemical synthesis” ü Practice ü Practice ü Practice ü Practice Sample Problem #1 H O from ... Hint: Thorough reaction knowledge increases flexibility and simplifies synthesis problems. Some problems might not be doable without good mastery of reactions!

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    • [PDF File]Practice Problems on SN1, SN2, E1 & E2 - Answers

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      Practice Problems on S N1, S N2, E1 & E2 - Answers 1. Describe the following chemical reactions as S N1, S N2, E1 & E 2. Draw a curved arrow mechanism for each reaction. NaI 3 3 Cl KCN DMSO CN Br NaOH H2O, heat BrH 2O OH I CH3CH2O-Na+ ethanol HI NaSH DMSO HSH Br HO KOH DMSO OTs NaNH2 NH3 TsO NH3 H2N O O CH CH3 TsO acetone O O CH CH3 I SN2 E2 ...

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    • [PDF File]PRACTICE EXERCISE – ORGANIC CHEMISTRY I Alkynes …

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      practice exercise – organic chemistry i alkynes synthesis and reactions for questions 1-4, draw a lewis or line-angle formula and give the iupac name. 1) (ch3)2c(ch2ch3)ccch(ch3)2 2) hccch2ch2ch3 3) ch3ch=chch=chccch3 4) brch2ch2ccch2ch3

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    • [PDF File]Organic Chemistry II

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      1.3 Synthesis of Ketones The use of H 2 CrO 4 or PCC in CH 2 Cl 2 will convert a 2 alcohol to a ketone Grignard reagents or organolithium reagents can convert a nitrile to a ketone. Examples are shown below: 1.4 Synthesis of Ketone Example Note that PBr 3 replaces an OH with a Br and does not have rearrangements It is useful for creating alkyl ...

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    • [PDF File]Review of Organic Chem II - Minnesota State University ...

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      Organic Chemistry II Review Jasperse Some Fundamental Stability/Reactivity Principles 3 2. Product Stability/Reactivity: The more stable the product, the more favorable its formation will be.In terms of rates, this means that the more stable the product, the faster the reaction.

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    • [PDF File]Final Exam for Organic II 200pts(Weighted as 300)

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      Final Exam for Organic II 200pts(Weighted as 300) Name Good luck all round! 1) Identify the class of compounds each of the following molecules belong to (15pts). ROH ROR O R C O H R C O O-H R C O O C O C R O O-R RCN R C O NR 2 C H N O 2) For each of the amides and amines state whether they are primary, secondary or tertiary (4pts).

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