Design syntheses to produce the following compounds starting withany alkyl halide with 3 or fewer carbons...
Design syntheses to produce the following compounds starting withany alkyl halide with 3 or fewer carbons and butadiene. You may useany any inorganic reagents necessary. Note that once a compound hasbeen synthesized in one process it can be used in a different process ifyou reference where it was first made.
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Design syntheses to produce the following compounds starting
withany alkyl halide with 3 or fewer carbons...
Synthesis Experiment #2: Design syntheses to produce the following compounds starting with ethylene and any methyl...
Synthesis Experiment #2:
Design syntheses to produce the following compounds starting
with ethylene and any methyl halide. Note that once a compound has
been synthesized in one process it can be used in a different
process if you reference where it was first made.
Starting with Benzene and any alkyl halide with four or fewer carbons and any needed inorganic...
Starting with Benzene and any alkyl halide with four or fewer carbons and any needed inorganic reagents, show how you would synthesize the following compounds: a)m-bromoiodobenze b) m-chloroethylbenzene c)o-nitroalinine d) m-hydoxybenzoic acid e) p-methylbenzonitrile
Synthesize the following compounds from the given starting material. You may add on any alkyl/alkyl halide...
Synthesize the following compounds from the given starting material. You may add on any alkyl/alkyl halide under 6 carbons or any necessary inorganic reagent needed (this includes triphenyl phosphine (Ph3P). Draw all intermediates and reagents necessary to reach product. OH tar
Synthesize the following compounds from the given starting material. You can add on any alkyl/ alkyl...
Synthesize the following compounds from the given starting
material. You can add on any alkyl/ alkyl halide under 6 carbons or
any necessary inorganic reagent needed (this includes triphenyl
phosphine (Ph3P). Please draw all intermediates and
reagents necessary to get to the product.
OH سالن سل = ها را
Devise a synthesis of these compounds starting with 3-carbon alkyl halides. Show any necessary reagents and...
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. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each...
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
R-x 1. Prepare the following compounds from any simple alkyl halide having four carbons or less...
R-x 1. Prepare the following compounds from any simple alkyl halide having four carbons or less (can be branched, but no other functional groups), ethylene oxide, cyclohexane, and/or cyclopentane. Any other carbon-containing reactants must be synthesized from the above mentioned reagents! Show all steps and reagents.
Design an effective synthesis for each of the following amino acids starting from the compounds shown...
Design an effective synthesis for each of the following amino acids starting from the compounds shown on the left. You may also use any monofunctional organic compound containing four or less carbon atoms, and any inorganic reagents in your syntheses.
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You...
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You may use any other readily available alkyl halides, solvents and reagents as necessary. More than one step is necessary. Show all intermediates, reactions, reagents and conditions clearly. It is not necessary to show the mechanism. HCECH HCECH , X HCECH HC=CH M H OHC (30 marks)
Starting only from organic reagents of 4 carbons or fewer, propose an efficient synthesis for the...
Starting only from organic reagents of 4 carbons or fewer, propose an efficient synthesis for the molecule below. You may use any necessary solvents and inorganic reagents, and can assume that all products can be isolated as needed. If only one product is to be taken on to a new step, indicate which one.
Synthesis Experiment #2:
Design syntheses to produce the following compounds starting
with ethylene and any methyl halide. Note that once a compound has
been synthesized in one process it can be used in a different
process if you reference where it was first made.
Synthesize the following compounds from the given starting material. You may add on any alkyl/alkyl halide under 6 carbons or any necessary inorganic reagent needed (this includes triphenyl phosphine (Ph3P). Draw all intermediates and reagents necessary to reach product. OH tar
Synthesize the following compounds from the given starting
material. You can add on any alkyl/ alkyl halide under 6 carbons or
any necessary inorganic reagent needed (this includes triphenyl
phosphine (Ph3P). Please draw all intermediates and
reagents necessary to get to the product.
OH سالن سل = ها را
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
R-x 1. Prepare the following compounds from any simple alkyl halide having four carbons or less (can be branched, but no other functional groups), ethylene oxide, cyclohexane, and/or cyclopentane. Any other carbon-containing reactants must be synthesized from the above mentioned reagents! Show all steps and reagents.
Design an effective synthesis for each of the following amino acids starting from the compounds shown on the left. You may also use any monofunctional organic compound containing four or less carbon atoms, and any inorganic reagents in your syntheses.
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You may use any other readily available alkyl halides, solvents and reagents as necessary. More than one step is necessary. Show all intermediates, reactions, reagents and conditions clearly. It is not necessary to show the mechanism. HCECH HCECH , X HCECH HC=CH M H OHC (30 marks)
Starting only from organic reagents of 4 carbons or fewer, propose an efficient synthesis for the molecule below. You may use any necessary solvents and inorganic reagents, and can assume that all products can be isolated as needed. If only one product is to be taken on to a new step, indicate which one.
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