Write reaction equation for the reaction you did following the template given below. Use the actual...
For the stereoisomers below, use the R/S configuration given in the compound name to finish drawing the structure by connecting the appropriate groups. Be sure to specify the stereochemistry via wedge-and-dash bonds. If needed, you may restore a module to its orignal state by clicking on the module and then clicking on the red over-under arrows.
1. Use the template below to summarize all methods to prepare alcohols. Reagent Reaction Scheme Substrate (s) Comments Functional group of the product Mechanism (type) Stereochemical Implications Alkyl Halide hydroxide alcohol R-Br + oH — R-OH + Br® Sw2 yes, with secondary R-X. Inversion of stereochemical configuration Works for CH3-X, primary and secondary Alkyl Halide Alkene
Draw the structure of the compound you would expect from SN2 reaction of the molecule below with NaCN. Use the wedge/hash bond tools to indicate stereochemistry. Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it. You may use the OWL references to look up acidities if you want to compare leaving groups.
use condensed structural formulas to write the balance equation for the reaction of salicylic acid with acetic anhydride. Use the models to demonstrate the reaction use condensed structural formulas to write the balance equation for the reaction of salicylic acid with methanol. Use the models to demonstrate the reaction Describe the appearance of aspirin product REPORT SHEET: ASPIRIN Name Partner(s) Date Section Instructor A. Molecular models Use condensed Ne condensed structural formulas to write the balanced equation for the reaction...
Use the Fischer projection below to answer the following questions сн. Br- H H- Br CH,CH, (a) Write the IUPAC name for this molecule using the R/S notation (b) Draw the skeletal structure of the mirror Image, le the enantiomer, of the molecule whose Fischer projection is given above. (Show one wedge bond, one dashed bond, and two sticks attached to the chiral carbon. Show the hydrogen atom bonded to the chiral carbon atom as either a wedge or dash...
PRE-LAB QUIZ for EXPERIMENT 27 Name 1. In Experiment 27, a modified Perkin reaction is performed. The Perkin reaction is a carbonyl condensation reaction that is related to the Claisen condensation and aldol condensation. In this experiment, the reactants are benzaldehyde and 3-benzoylpropionic acid with sodium acetate and acetic anhydride as catalysts. Draw the structures of these compounds in the space below. benzaldehyde 3-benzoylpropionic acid acetic anhydride 2. The first step of the reaction is the formation of the mixed...
Extend the code from Lab6.A template is given to you with CircleHeader.h, Circle.cpp and CircleMain.cpp Use the same Circle UML as below and make extensions as marked and as needed. Given below is a UML for the Painting Class. You will need to write PaintingHeader.h and Painting.cpp. The Painting Class UML contains a very basic skeleton. You will need to flesh out this UML and add more instance variables and methods as needed. You do NOT need to write a...
The synthesis of triphenylmethanol via the grignard reaction is given by the following equation (below): A student decides to perform the above reaction. She starts with 200 mg of bromobenzene (M.W. = 157) and uses 45 mg of Mg (M.W. = 24.3) and 0.36 g of benzophenone (M.W. = 182). a. Calculate the limiting reagent b. Calculate the theoretical yield of triphenylmethanol (M.W. = 260.3) c. She obtains 0.172 grams of of the product. What is her actual yield? d....
Please tell me if i have part (a) correct or not? and answer part (b) for me please with clear hand wrriten please. Question 8) A) Below is a reaction scheme you performed in lab to reduce 4-+-butylcyclohexanone to the corresponding cis and trans secondary alcohol isomers. In lab you used NaBH4 to reduce the ketone, but state whether it is also possible to use LiAIH4. If so, why did we choose NaBHs instead of LiAIH? OH NaBH4 MeOH 个个and...
4. Use the following reaction equation to answer the questions below; B(OH) Pd/C, K,co microwave. Mass ( % yeild actual actual-ss。 Compound mp (°C) 216-219 50-52 891 Vol (mL) phenylboronic acid 4-bromoacetophenone L0.597 potassium carbonate 5% palladium on 0.366 1.244 018 0.967 21 4 carbon TBAB (BUANBr) Water (15 points) The actual yield for the above experiment was 550 mg. Calculate the theoretical and percent yield. What is the name for this reaction? For full credit, you must show the...