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- This question has multiple parts. Work all the parts to get the most points. a Draw all of the monochlorination products that you might obtain from the free-radical chlorination of 2,2,4-trimethylpentane. You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.Using dash–wedge notation to designate stereochemistry, draw (R)-pentane-1,2-diol.In the drawing area below, create an acetal with at least 3 methoxy groups, and a total of 5 carbon atoms.
- Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.C6H5CO2CH2C6H5 can be synthesized by an SN2 reaction. Draw the structures of the alkyl chloride and nucleophile that will give this compound in highest yield. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include all valence lone pairs in your answer. Separate multiple reactants using the + sign from the drop-down menu. When a metal counterion is needed, use Na+, but draw it in its own sketcher.Draw the structure of the organic product of the reaction between cyclohexene and H2SO4, H2O. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Separate multiple products using the + sign In cases where there is more than one answer, just draw one. Please make your answer clear. I did not understand the first answer because it was hand -written
- Draw the major organic product(s) in the sketch pad below.I need help on letter 4E only. I drew the structural form already*Please draw an alkane that has at least one primary, one secondary, and one tertiary carbon. Then take molecule and react it with F^2 (Identify all mono halogenated products for each reaction)
- Please help with row 2/question 2 ; the instructions for the specific column in row 2 are above row 1: Follow the instructions in each column. Hint for the last column: draw it with a wedge and again with adash – which gives the correct configuration?Start with condensed structural formula CH3-CH(OH)-CH(CH3)-CH2-CH(CH3)2 and react it first with H2SO4 and high heat, to produce a major substrate product. Then, take that major substrate product, and use it as the substrate of the next reaction, by reacting it with Br2 (in the presence of CH2Cl2 solvent), to produce the FINAL MAJOR substrate product. The complete correct condensed structural formula for the major substrate product after reaction step 1 is ___________. (If no new product is formed in this step, type "no reaction.") The complete correct condensed structural formula for the final major substrate product (after reaction step 2) is __________ . (If no new product is formed in this step, type "no reaction.")For some questions you will need to use the special periodic table attached in the images! Treat Je, Qu, Ap, and Bg as NONMETALS! Classify each of the following alcohols as primary (1°), secondary (2°), or tertiary (3°)? Look at attached images (Please show work so I can understand going forward)