(a)
CH3-CH2-CH2-CH2-CH(Br)-CH3 + aq. KCN ------------> CH3-CH2-CH2-CH2-CH(CN)-CH3 + KBr
2 - Bromohexane 2 - Methylhexanenitrile
(b)
CH3-CH2-CH2-CH2-CH2-CH2-Br + CH3ONa ----------> (+/-) CH3-CH2-CH2-CH2-CH2-CH2-OCH3 + NaBr
1 - Bromohexane sodiummethoide 1 - methoxyhexane
(c)
CH3-CH2-CH2-CH2-CH2-CH2-Br + alc. KOH -----> CH3-CH2-CH2-CH2-CH=CH2 + H2O + KBr
1 - Bromohexane 1 - Hexene
(d)
CH3-CH2-C(CH3)(Br)-CH2-CH3 + aq. NaOH ------> CH3-CH2-C(CH3)(OH)-CH2-CH3 + NaBr
3-Bromo-3-methylpentane 3-Methyl-3-pentanol
2) Prepare each of the following from any C,H13Br starting material. (Show your starting material &...
show stepwise how you would prepare the following compounds from the provided starting material and any other organic or inorganic compound. in order to have full credit you mush show all the reactions conditions and the structure of your oroducts in each transformation (30 points) Show stepwise how would you prepare the following compounds from the provided starting material and any other organic or inorganic compound. In order to have full credit you must show all the reaction conditions and...
prepare the following compound from 2 carbon starting material . Phepare the following compound from any 2 carbon starting material and needed reagents. 2 Prepare the following compound from cyclohexanone and any I or 2 carbon starting material and needed 2 Prepare te following compound from cyclohexanone and any 1 or 2 carbon starting material and needed reagents
Organic Chemsitry show stepwise how would you prepare the following compounds from the provided starting material and any other organic or inorganic compound. In order to have full credit you must show all of the reaction conditions and the structure of your products in each transformation 041 => Оet HO Eto Oet
Use Dieckman cyclization to prepare the following compound from the indicated starting material. You may use any organic and inorganic reagents necessary. Your answer should clearly show your synthetic scheme complete with reagents and products for each step.
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
Show how to prepare to prepare the following using the substance CH, and any other a) CH CH CH CH CH from an alkene b) CH CH.CH,—0CHCH,CH from an alcohol w from 2-methyl-2-pentanol from 2-methy-2-pentano d) from 1-butene CH3 -CH-0-CH2CH3 СН2СН3
Show now you would synthesize the compounds listed in each set from the starting material given. You may use alcohol, alxene, alkyne that is four carbon atoms or less, any organic solvents necessary and in organic reagents as needed. It should take steps or less set 1 Starting with benzene, show how to make met a - biomobenzaldenyde met a- chloroaniline 1 - (4- nitiophenye) piopan - 1 - 01 1 - (3 - piopyephenye) piopan - 1 - 01...
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
2. Starting with butane, show, using chemical equations, how you could prepare a. 2-bromobutane b. 1-bromobutane Note: For the following targets, you may also choose to begin with either 2-bromobutane or the 1-bromobutane as prepared above without repeatedly showing how you made these two compounds. Be sure to choose the best starting material for each job! c. 1-butene d. e. 3-methylheptane f. 5-methyl-3-heptyne 2. Starting with butane, show, using chemical equations, how you could prepare a. 2-bromobutane b. 1-bromobutane Note:...
Can you show the mechanism thank you!!! Devise 2 different syntheses(list the starting materials and any reagents) of 3-methyl-3-pentanol. Each syntheses must involve a Grignard reagent.