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- Name the alkene below.Use only E/Z designators to indicate stereochemistry.Give typed explanation Predict the major products of this organic reaction: H H₂ Pt 4 Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. C™ с X 3 c+What are the reagents used to convert 2-butyne to C4H8? What are the products when that C4H8 is mixed with OsO4, and H2O (the formula will be C4H10O2 racemic)? What is the product when C4H8 is mixed with RCO3H, and H2O (the formula will be C4H10O2 meso)?
- Compound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yneDraw the structure(s) of the major organic product(s) of the following reaction. You do not have to consider stereochemistry. If a compound is formed more than once, add another sketcher and draw it again. 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.Ethers: Reaction of 1-methoxy-2- methylpropane and HI, heat. Draw the organic product or products formed when the structure shown below is heated with HI. If no reaction occurs, draw the starting material. Interactive 3D display mode
- Consider a reaction where cis-but-2-ene is treated with sO followed by NaHSO/H, O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.Consider a reaction where cis-but-2-ene is treated with a peroxy acid followed by OH- /H20. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.Consider a reaction where cis-but-2-ene is treated with OsO4 followed by NaHSO3/H2O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
- The 1,2‑dibromide is synthesized from an alkene starting material. Draw the alkene starting material. Clearly, show stereochemistry of the alkene.- For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H2SO4H2SO4, then draw the structure of the major product of the elimination. (Picture 1): Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate. Note: HSO−4HSO4− is formed from step 1, but not shown. (Picture 2): Step 3: Use a curved arrow to show the carbocation rearrangement. Step 4: Draw curved arrows to show the elimination to form the major product. Water is added as a base. - Draw the major product of the elimination. H3O+H3O+ has been pre‑drawn for your convenience.1. When you add H-Br in a terninal alkene, the product has the rule od Markovnikov? 2. The type pf intermetary thag forms when we add HgSO4/H2SO4/H2O in an alkyl is? Please solve my both questions.thank you.