19.33 (a) Give an acceptable name for compound C. (b) Draw the organicproducts formed when C is treated with each reagent: [1] H3O+; [2] ¯OH,H₂O; [3] CH3CH2CH2MgBr (excess), then H2O; [4] LiAlH4, then H₂O.C

(a) Name for Compound CThe name 3-cyanoheptane (2-ethylhexanenitrile). The compound has a…

Answered: 19.33 (a) Give an acceptable name for…

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter15: Carboxylic Acids And Esters

Section: Chapter Questions

Problem 15.55E

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a.) Give an acceptable name for compound C. (b) Draw the organicproducts formed when C is treated with each reagent: [1] H3O+; [2] −OH,H2O; [3] CH3CH2CH2MgBr (excess), then H2O; [4] LiAlH4, then H2O.
Provide reagents
17
complete the reactiona and draw it out
Write chemical equations of the reactions of ethanoic acid with(a) Sodium(b) Sodium carbonate(c) Ethanol in the presence of conc. H2SO4
Provide the correct structure from the IUPAC name. (a) 2-aminocyclopropanecarboxylic acid (b) 3-mercapto-5-oxoheptanal (c) Propyl 2,2,4-trimethyloct-4-enoate (d) 4-oxocycloheptanecarbaldehyde (e) N,N,4,4-tetraethylhexanamide (f) Acetic pentanoic anhydride (g) Acetyl chloride (h) Methyl 3,3-diethyl-6-octynoate
Provide reagents
The odor of ripe bananas and many other fruits is due to the presence of esters. For example: Banana oil (isopentyl acetate) (a) Write the name (common or IUPAC) of the ester responsible for the fragrance of the following: pineapple, orange, apple, peach, & lavender (b) Choose one fragrant from (a) and name the alcohol and the carboxylic acid needed to synthesize this ester. (c) Show the detailed mechanism of the Fischer Esterification reaction that will be involved in the synthesis of the fragrant you have chosen in part (a).
21.41 Identify a systematic (IUPAC) name for each of the following compounds: (a) OH (b) NH2 (c) CI
18.18 Provide a structural formula for the product from each of the following reactions. (a) (c) (e (1) LDA (2) CH,CH,I NaH CI (b) (d) O. (f Br, CH,CO,H Br, (excess), NaOH
19.62 Naltrexone is used to help recovering narcotic addicts stay drug free. HO O OH naltrexone LO1,6,7 (a) Label and name all the functional groups. Where relevant, indicate whether the group is primary, secondary or tertiary. (b) Upon addition of dilute hydrochloric acid solution, naltrexone forms a water-soluble salt. Draw the structure of this salt.
The hydrocarbon fluorene was treated with potassium t-butoxide in an acid-base reaction, giving the fluorenide anion and t-butyl alcohol. (a) Which way does the equilibrium lie, and by how much? b) What is the proportion of the fluorenide anion to fluorene? (c) Why is fluorene so highly acidic, considering the pKa of an average alkane is above 50?

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19.33 (a) Give an acceptable name for compound C. (b) Draw the organic products formed when C is treated with each reagent: [1] H3O+; [2] ¯OH, H₂O; [3] CH3CH2CH2MgBr (excess), then H2O; [4] LiAlH4, then H₂O. C