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- Draw a cross section of a double bond of ethene. Label each lobe appropriately.
Step by step
Solved in 2 steps with 1 images
- Part a) Draw step by step arrow pushing mechanism for formation of X. Please make it neat and detailed. Part b) Draw Y.Start with a cyclohexane. Add double bonds at the 1st, 3rd, and 5th carbons. Add two methyl groups with 1 carbon separating them. Add 1 bromine on the carbon that is in between the two methyls.Be sure to answer all parts. Draw the structure corresponding to each IUPAC name. a. 6-ethyl-2-octyne I I 1 I -CH₂ I I H₂C edit structure... b. 5,6-dimethyl-2-heptyne I I I I I draw structure...
- 3. Draw out 3-methylpentane. Use lower-case letters to label each TYPE of hydrogen (i.e., those that would lead to a different product) on each compound.a) This alkene can be prepared via Wittig reaction. Draw structural formulas for the aldehyde and the Wittig reagent. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Draw the Wittig reagent in the ylide form. • If more than one combination of Wittig reagent and aldehyde is possible, draw only one set. b) How would you convert the alkene to a epoxide? MCPBA c) How many chiral centers are present in the epoxide? V How many stereoisomers are possible in the epoxide that you formed in b)?a) This alkene can be prepared via Wittig reaction. Draw structural formulas for the aldehyde and the Wittig reagent. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Draw the Wittig reagent in the ylide form. • If more than one combination of Wittig reagent and aldehyde is possible, draw only one set.
- Draw the structure of the given compound. Identify if the given name is correct of incorrect. If not, provide the correct IUPAC name of the compound. Don’t use CIS/TRANS or E/Z in naming the compounds. 1) 6-PROPYLCYCOHEPTENE 2) 7-BUTYNYLDODEC-1-ENE Note: need answers immediately. Will give a good rate right away as well.Determine the number of carbons present in the compound based on the base name. Draw the carbon chain and include any double or triple bonds if indicated in the suffix of the base name. Number each carbon. The carbons can be numbered from left to right or right to left. Draw any substituents on the corresponding carbon atom for which is indicated in the name. Refer to Figures 4 and 5 in the background for a visual representation of numbered carbons with corresponding substituents. Check that each carbon atom has a total of 4 bonds.Draw the structure corresponding to each IUPAC name.a. (Z)-4-ethylhept-3-eneb. (E)-3,5,6-trimethyloct-2-enec. (Z)-2-bromo-1-iodohex-1-ene
- Structure 4: Draw the structure with a postively charged oxygen. Select Draw Rings More Erase C H. H,C CH, H,C CH,Draw the molecule on the canvas to show the product.Draw the structures of the of the starting materials needed to make 2-methylhept-3-yne or 2-methyl-3-heptyne. The starting materials may be any bromoalkane having five carbons or fewer. Draw Starting Material A. The starting hydrocarbon must be a bromoalkane with five carbons or fewer. Draw reagent C which must be a bromoalkane with five carbons or fewer.