provide methods for preparing following compunds by the Grignard method::
1 & 2)
using grignards you could start out with 1-bromoethane, then add Mg in a polar solvent without H bonds, so diethyl ether is usually used. then you would have CH3CH2-+MgBr which is your grignard. now you would have to add propanal which is CH3CH2-CHO. the grignard attacks the carbonyl and after adding some acid you get the alcohol, and you have 3 pentanol.
to get 3-methyl-3-pentanol, do the same work up,
except instead of adding propanal, add 2-butanone, then acid and
you have your product. it is important to remember that you cannot
have acidic protons in grignard reactions, so adding the acid should be the very last step, and it
could just be H3O+.
treating propanal with ethyl magnsium bromide
and then dilute acid will yield 3 pentanol
C2H5MgBr + O=CH-C2H5-------
C2H5-CH(OH)-C2H5
treating 2 -butanone with ethylmagnesium bromide
and then dilute acid will generate 3-methyl 3
pentanol
C2H5MgBr + CH3-CO-C2H5---- C2H5
-C(CH3)(OH)-C2H5
3)
4)
provide methods for preparing following compunds by the Grignard method:: Provides methods for preparing the followi...
Provide methods for preparing the following compound, by .he Grignard method identify the starting material for preparing the Grignard reagent, and the reactant(s) it must react with in order to produce the target compound.
Provide methods for synthesizing the following compounds using only a Grignard reaction, plus any necessary workup. In each case the Grignard reagent, cyclohexylmagnesium bromide, must be used in the synthesis. Express these syntheses in the form of balanced equations, using structural formulae showing all reagents and any specific conditions required. a) Cyclohexylmethanoic acid b) 1,1-dicyclohexyl-1-ethanol c) cyclohexane
Grignard reagents and Alkyl lithiates are moisture sensitive. What is the major organic product obtained if the following organometallic compounds come in contact with deuterated water?
draw the structures of the following compunds: 1. Draw the structures of the following compounds: a. 3-ethyl-4-methyl-2-hexane 12V DAUI orgian antivollotor b.2-chloro-butyl acetate HDHO c. Ethylbenzene HOHO d. 2-methyl-3-pentanol HD HO-HD-HO-HO HD e. 2-methylpropyl methyl ether
A) Budgeting and Budgetary Control (Three methods of preparing cash budget; Receipts and Payments Method, Adjusted Profit and Loss Method, Balance Sheet Method - which one is more practical and fit for the purposes of businesses and why?
Outline two methods for preparing isopropyl methyl ether by a Williamson synthesis. One method gives a much better yield of the ether than the other, explain your answer.
Which of the following Grignard reagents can be made? For the compounds that are not feasible Grignard reagents, explain why the compound will not work.(Include a mechanism if this would be helpful in your explanation.) MgBr MgBr MaBr MgBr H Lowon MgBr MgBr
Draw the Grignard reagent you'd expect to form from the following reaction Provide the product you'd expect from the following reaction? OH SOCI pyridine
An example of 4 main methods of speech delivery. Explain each method of delivery. Provide examples of the situations that these methods would be used.
4. Provide the possible combinations of Grignard reagent(s) and carbonyi compound(s) that will yield the following alcohols: (20pts) a) 1-phenyl-2-propanol b) 3.3-dimethyl-2-phenyl-2-butanol