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.
1. Draw the structure of any secondary alkyl halide containing at least six carbons. 2. Name...
Be sure to answer all parts. Part 1: Identify the a and ß carbons in the alkyl halide. 2 1 Br The a carbon(s) include: 0 1 0 2 0 3 0 4 The ß carbon(s) include: 0 10 20 30 4 Part 2 out of 2 Draw the possible elimination products formed when the alkyl halide is treated with K+ COC(CH3)3. Elimination product formed when carbon 1 is the ß carbon: draw structure ... Elimination product formed when carbon...
Draw the possible elimination products formed when the alkyl halide is treated with K-OC(CH). Elimination product formed when carbon 1 is the ß carbon: draw structure ... Elimination product formed when carbon 2 or 4 is the ß carbon: draw structure...
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.
1. Circle the two alpha carbons and box the two leaving groups in methamphetamine. methamphetamine 2. Methamphetamine reacts with Br. Draw structure of the two possible products. (Hint: nucleophile reacts at each alpha carbon) 3. Assume the secondary alpha carbon in methamphetamine undergoes loss of leaving group (first step of a SN1 mechanism). Draw the structure of the carbocation.
Write balanced equations and draw the structure for any reactions undergone by each alkyl halide with Nal/Acetone: 2-bromobutane, 2-bromo-2-methylpropane, 1- bromobutane, bromocyclohexane, 1-bromoadamantane and write out mechanism for the reaction 2-bromobutane in NaO/Acetone
Write balanced equations and draw the structure for any reactions undergone by each alkyl halide with AgNO3/ethanol 2-bromobutane, 2-bromo-2-methylpropane, 1-bromobutane, bromocyclohexane, 1-bromoadamantane and write out mechanism for the reaction of 2-bromobutane in AgNO3/Ethanol
Write balanced equations and draw the structure for any reactions undergone by each alkyl halide with NaI/Acetone: 2-bromobutane, 2-bromo-2-methylpropane, 1-bromobutane, bromocyclohexane, 1-bromoadamantane and write out mechanism for the reaction 2-bromobutane in NaO/Acetone
1) Draw Hayworth projections for lactose and sucrose. Identify the monosaccharides present and the type of glycosidic bond in each molecule. Using arrows, indicate the location ppei carbons, and identify each nomenig carbon as a heminscta or an acetal carbon. 2l Draw the stnuctur statriacyllyeralcoataining livaleic Jivalenik. and.oleis acid, 3) Write the balanced chemical equation (using structures) for the saponification of the triacylglyseral in problem 2. 4) Draw the structure of a lecithin containing palmitoleic and oleic acids. Cirele the...
Using line structure, draw a hydrocarbon molecule that has (all three) : at least 5 carbons in the parent chain at least 1 carbon-carbon multiple bond at least 2 branches Write the correct molecular formula for your molecule (CxHy). Write the correct name for your molecule.
1.(a) (2pts.) Draw the structural formula for each amine. (b) provide the IUPAC name the structure below 4-aminobutanal (R)-2-butanamine 2. (6 pts.) Consider the Grignard reaction shown below which forms a C-C bond via an Aw step. In box A, draw the structure of the nucleophile involved in the A step and highlight the nucleophilic atom. In box B, draw the structure of the electrophile involved in the Aw" step and circle the electrophilic atom. In box C, draw the...