Draw the structures of all the possible products that can be obtained from the dehydration of 2-methylcyclohexanol. Using curved arrows, write a detailed mechanism to show how each product is formed. Indicate which product would be the major one.

Hello, I do not understand these questions and I am stuck. May I get help please please?? Question: Draw the curved arrow mechanism for the following reactions

Can you prepare diisopropyl ether as the major product by heating 2-propanol in the presence of sulfuric acid? O Yes, because these conditions promote the substitution reactions. O Yes, because these conditions are highly favorable for O No, because secondary and tertiary alcohols undergo elimination reactions in these conditions. O No, because secondary and tertiary alcohols do not react in the presence of sulfuric acid.

CH3 གོན་ནི། ཡོན་ Br₂, H₂C CH₂Br H3C CH3 H₂C CH3 Aldehydes and ketones can be halogenated at their a-position by reaction with Cl₂, Br2, or 12, under acidic conditions. Using Br₂ under acidic conditions, an intermediate enol is formed which adds bromine at the a-position. The reaction stops after the addition of one bromine because the electron-withdrawing halogen decreases the basicity of the carbonyl oxygen, making the protonation less favorable. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions :0: :OH н-он H-OH₂ H₂O H₂C. H3C. CH3 CH3 H3C CH3 H3C CH3 Σα

Suggest a step by step mechanism for this reaction.

4. Draw the organic products of the reactions of (R)-2-iodobutane with azide ion and methanol. Draw allstereoisomers expected to form. (R)-2-iodobutane Na*N3* CH3OH

Draw the principal organic product for the reaction when 2-bromopropane is treated with lithium in diethyl ether, followed by copper(I) iodide and then 1-bromoethane. Click and drag to start drawing a structure. X

In the synthesis of 1,2-dibromopropane from propan-1-ol: how many steps does it take in the shortest route?

Part a can you please help ?

IF esize this compound by the → t-butyl ethyl ether Show the steps necessary to synthesize this compound by a rignard reaction. Start with an alkyl halide; after that you can add any organic or inorganic compound. → 1-hexanol Consider the following compounds: