When 2,2-dimethylcyclohexanol reacts with acid in water, multiple products form. One of these products is shown below. Provide a complete mechanism for the following transformation usin

Using acetylene as your only source of carbon atoms, identify a synthetic route for the production of 1-bromobutane. First, select the reagents necessary for the transformation shown, using no more than four steps in the synthesis. In part 2, you will synthesize any carbon reagents (other than acetylene) that were used in the synthesis. The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagent(s) in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer.

Show all the reactions stepwise to achieve the following transformation. Also clearly write down the curved-arrow mechanism for each step. Br steps? OH

Provide a synthesis for the target molecule shown below, starting with compounds that contain no more than two carbon atoms. Show your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents.

Using acetylene as your only source of carbon atoms, identify a synthetic route for the production of 2-bromobutane. First, select the reagents necessary for the transformation shown, using no more than four steps in the synthesis. In part 2, you will synthesize any carbon reagents (other than acetylene) that were used in the synthesis. H- -H Br The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagent(s) in the correct order, as a string of letters (without spaces or punctuation, such as “EBF"). If there is more than one correct solution, provide just one answer. A В МeONa NaNH2 t-BUOK E F EtBr H2, Lindlar's cat. Br2, hv G H HBr, ROOR H2, Pt HBr

Propose a sequence of reactions to prepare the specified target compound from the indicated starting materials.  All of the carbon atoms in the target must originate in the specified starting materials.  Keeping this restriction in mind, you may use any other organic or inorganic reagents necessary to complete the synthesis. It is only necessary to show the overall transformations involved in your proposed synthesis.

Solve with explanation need

Draw a detailed reaction mechanism for the following transformation: NaOH To obtain the complete score you must clearly indicate all the intermediaries and the correct movement of electrons.

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ELO ots Propose a sequence of reactions to synthesize the target compound below from the indicated starting materials. You may use any other organic and/or inorganic reagents necessary to complete your synthesis, but all carbon atoms in the target must be derived from the starting materials specified. It is only necessary to give overall transformations in answering this question. Please DO NOT provide curved arrow mechanisms for the reactions that you use. Please note that all carbon atoms in the target must originate from any of the indicated starting materials. You may not need to use all of these starting materials to complete the synthesis. OH CH3I CH;CH,Br CH;CH2CH,Br EtO `CH3 TARGET 3-Ethyl-2-hexanol You may only use these compounds as necessary as the sources for all C atoms in the target Your ansa ded in the single ndf file that vou upload for the "Exam 5 File Submission"