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please help solve all 1. What is the name of the reaction? 2. Identify the number...
solve and answer all 5 questions please 1. What is the name of the reaction? 2. Identify the number of unique carbons and protons in each of the starting materials and in the product 3. Predict the product of the reaction. 4. Illustrate the mechanism of the reaction based on notes or book as a reference. You can use the structures from the book/notes instead of your assigned compounds, especially if your starting materials are complicated. 5. Give advice on...
Please help me and answer all 5 questions. 1. What is the name of the reaction? 2. Identify the number of unique carbons and protons in each of the starting materials and in the product 3. Predict the product of the reaction. 4. Illustrate the mechanism of the reaction based on notes or book as a reference. You can use the structures from the book/notes instead of your assigned compounds, especially if your starting materials are complicated. 5. Give advice...
help please 9-1 Give the IUPAC name for the product of following reaction. HCI 9-2 Draw the reaction mechanism of the previous problem (9-1).
Please help with g and h 1. For each reaction below, identify the mechanism involved, and draw the mechanism for the reaction including intermediates (no transition states required). There may be more than one product, if so, draw them both (watch out for rearrangements), Draw the mechanism below the reaction, and then ill in the products on the right side of the equation. Plesse work this out on another pie paper, then transfer your answer to this sheet.
a) Give all the major product(s) and stereochemistry where applicable. b) Identify and name all the functional groups in the product(s). c) Propose a reaction mechanism for each reaction. LiAlH4 CH3OH/H sono finit parents H2O/H30* N2 1 2 H20 CH3ONa CH3OH NaCN/H20 NH3 1. CH3MgBr 2. H20
1. A Robinson annulation is a reaction that involves: (i) a Michael addition of an enolate onto an ,ß-unsaturated enone followed by (ii) an intramolecular aldol reaction. The molecule shown below (cyclohexenone X) can be made through two different Robinson annulation reactions. (A) Show the two different sets of starting materials (i.e. ketone 1 &a,p-unsaturated enone 1 and ketone 2 & a,B-unsaturated enone 2) for each Robinson annulation. Draw the reagents/reaction conditions. (B) Then pick one set and draw an...
Give the name of the alkene shown below. Show the mechanism of the reaction below. Identify all intermediates and the product. Give a specific reason as to why the product is optically inactive. н-Вr н НС CH3 raw the mechanism for the reaction of I-Br with 1-methylcyclohexene showing all intermediates and oduct with proper stereochemistry. Explain why the product is optically inactive.
please help me solve these questions. i am very confused. Draw the step by step reaction mechanism and predict product(s) of the following reaction? (10 pts) OH
Please help with these questions, there may be more than 1 correct answer! The final product in equation (ii) is P. How many unique protons are there in P? он CH 3 СНз O 5 0 6 0 8 Which statements correctly describe the relationship between unique protons in a molecule and peaks in the molecule's 1H NMR spectrum? Check all that apply The number of 1H NMR peaks is exactly equal to the number of unique protons. The number...
4. (15 Points) Pericyclic Reactions: The transformation below can be described as a pericyclic reaction followed by a polar-acidic mechanism, where the acid is not shown because it is picked up from the environment. (a) Start by redrawing the starting material below, and show how the pericyclic reaction occurs with curved arrows. (b) Specify the type of pericyclic reaction it represents and the name reaction. (c) If you've done the pericyclic reaction correctly, your product will be an enol. From...