Draw the chemical structure of 10 alkyl groups starting from methyl (1 carbon) to decyl (10...
1. Draw the structure of any secondary alkyl halide containing at least six carbons. 2. Name it. 3. Circle the alpha carbon. 4. Draw box around all the beta carbons. 5. Draw the product(s) for the elimination reaction product for your choosen alkyl halide.
pleqse explain and draw structures! Thank you! Propose a synthetic route using only ethyne and methyl halide as your only source of carbon (all alkyl halides with 2 or more carbons needed should be synthesized) 10. 11. HO 12. Propose a synthetic route using only ethyne and methyl halide as your only source of carbon (all alkyl halides with 2 or more carbons needed should be synthesized) 10. 11. HO 12.
Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either from an ester and two moles of a Grignard reagent, or from a ketone and one mole of a Grignard reagent. Use retrosynthetic analysis to suggest one path of each type to synthesize 3-methyl-3-pentanol. (Click and drag the appropriate image to the correct position in the following reactions.) Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either...
Devise a synthesis of these compounds starting with 3-carbon alkyl halides. Show any necessary reagents and reaction conditions. All carbons must ultimately come from the 3-carbon alkyl halides. Once you have made a new compound, you may reuse it without making it again. a) Propanone b) Butanoic acid c) 3-hexene
Please help! I can't seem to get it, thanks! 4) Draw the indicated alkyl groups below. Draw the group Number of carbons in the group Group methyl Group ethyl •CH3 Propyl Isopropyl Butyl Sec-butyl Tert-butyl Lunda Lunda Lada Lamba mabanda nie malu nhu anhund Isobutyl Hexyl Isohexyl Cyclopenty cyclopropyl -
Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either from an ester and two moles of a Grignard reagent, or from a ketone and one mole of a Grignard reagent. Use retrosynthetic analysis to suggest one path of each type to synthesize 2-methyl-2-butanol. (Click and drag the appropriate image to the correct position in the following reactions.) Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either...
has two alkyl groups attached to N and the six- lishes the root: It is a cyclohexenamine. The methyl group that is attached to N is treated as a substituent and is given Nas its locator. In the second molecule, the longest carbon chain that is attached to N has five carbons, so it is a pentanamine. There is one ethyl substituent that is attached to N, so it appears as a prefix and is given the locator N There...
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate was formed. 2. Draw and compare the structures of acetylsalicylic acid and methyl salicylate. Circle and name the functional groups in both compounds. 3. The fragrance of apricots is due to the ester pentyl butanoate. Write the equation for the synthesis of this ester from the acid and the alcohol. 4. Give examples and names of any other compounds that contain the functional groups...
Can someone correct the alkyl groups I placed on structure A, as well as the ring flip on structure B, and the resulting conformer? This is very confusing to me. 8. A perspective drawing of 1-chloro-2-isopropyl-4-methylcyclohexane is shown below. Place the alkyl groups on structure A, then perform a ring flip and draw the resulting conform
Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either from an ester and two moles of a Grignard reagent, or from a ketone and one mole of a Grignard reagent. Use retrosynthetic analysis to suggest one path of each type to synthesize 3-methyl-3-pentanol. (Click and drag the appropriate image to the correct position in the following reactions.)