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when acid anhydride reacts with excess amine and forms the amide and the ammonium salt as follows
Please answer all parts for good rating! 2) Predict the products and provide the complete arrow-pushing...
Please answer all parts for a good rating!
Predict the product(s) for each of the following reactions. Pay attention to stereochemistry. In each case, a reaction occurs, even if it is simply an acid-base reaction А) HO но H+ NaOEt Он C) pH 4~5 NH2 BL 2) Predict the organic product(s) at each step in the following reaction scheme. Also provide the complete arrow-pushing mechanism for the full process. You may use -Ph as an abbreviation for a benzene ring...
Predict the products and provide the complete arrow-pushing mechanism for the reaction below. NaOEt EtOH
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A) Name the following compounds using IUPAC rules: B) Provide the structures for the compounds below: 4-bromobutanal acetophenone yy fty For the following reaction, provide the structure of the open- chain form of the compound (pay attention to stereochemistry) and the complete arrow-pushing mechanism for the reaction. open-chain form HO Starting with the compound shown and only alcohols (including diols) of three carbons or less, suggest a means by which to achieve the...
Please show complete arrow pushing mechanism for the following
reaction. The answer had three products and I am not sure why.
2. (30 Points) Provide a complete arrow pushing mechanism of the following reaction to demonstrate how all the products are formed. consell you. Cound.o.o (enantiomer) (enantiomer)
2. (30 Points) Provide a complete arrow pushing mechanism of the following reaction to demonstrate how all the products are formed. da cabou Loom. Coord.o.o (enantiomer) (enantiomer)
Arrow Pushing Mechanism Help
Mechanisms & Development Provide the complete arrow-pushing mechanism for the following reaction. HT, H2O НО ОН
5(a). Predict the product for the following reaction.
(b). Provide an arrow-pushing mechanism for the reaction above that
accounts for the formation of the product. Explicitly include all
non-bonding electrons and charges. Indicate whether each step is an
initiation, chain propagation, or termination.
(c). An additional product, shown below, is formed in the reaction
from part (a). Provide an arrow-pushing mechanism that accounts for
the formation of the
additional product. (You may start from any intermediate from part
(b))....
a) complete the curved arrow electron-pushing mechanism and
predict the major organic product of the reaction when
1-chloropentane is treated with hydroxide in ethanol as shown
below.
a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the Draw the structure of the organic product formed in the reaction. Draw lone pairs. conversion to the product. CH3CH2OH -CI...
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The following reaction will not result in complete conversion to the amide compound. Suggest all of the products (the main organic products as well as any by-products) and indicate the number of moles of each product formed and the approximate number of moles of each reagent remaining. The reaction takes place in an inert (non-reactive) solvent. NH u. CI 1.0 mol 1.0 mol Suggest the reagents and steps needed to synthesize the following...