POST-LABORATORYQUESTIONS1. Effective mosquito repellents contain DEET (N,N-diethyl-3-methylbenzamide). If you were tosynthesize this compound, with what carboxylic acid and amine would you start? Draw theirstructures.CH3DEETOC-NCH₂CH3CH₂CH3H3CMetadone2. Metadone, a narcotic analgesic (shown below as the amine), is dispensed as its hydrochloride salt.Explain the use of the salt rather than the amine. Use the structure shown and convert it to thehydrochloride salt.N-CH3ogged

The concept used here is from basic organic chemistry. Process used here in both the question is…

POST-LABORATORY QUESTIONS 1. Effective mosquito repellents contain DEET (N,N-diethyl-3-methylbenzamide). If you were to synthesize this compound, with what carboxylic acid and amine would you start? Draw their structures. CH3 DEET O I C-N CH₂CH3 CH₂CH3 2. Metadone, a narcotic analgesic (shown below as the amine), is dispensed as its hydrochloride salt. Explain the use of the salt rather than the amine. Use the structure shown and convert it to the hydrochloride salt. N-CH3 H3C Metadone

POST-LABORATORY QUESTIONS 1. Effective mosquito repellents contain DEET (N,N-diethyl-3-methylbenzamide). If you were to synthesize this compound, with what carboxylic acid and amine would you start? Draw their structures. CH3 DEET O I C-N CH₂CH3 CH₂CH3 2. Metadone, a narcotic analgesic (shown below as the amine), is dispensed as its hydrochloride salt. Explain the use of the salt rather than the amine. Use the structure shown and convert it to the hydrochloride salt. N-CH3 H3C Metadone

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

1. NaOEt CO₂Et 2. H3O+ 3. heat Br H3C CO₂H CO2 H3C CO₂Et The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon chain by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN2 reaction with a primary alkyl halide, ester hydrolysis under acid conditions, and decarboxylation. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions 22 CX EtO₂C EtO₂C HOCH2CH3 HOCH2CH3 EtO₂C EtO₂C
. The following structure represents cortisol, an anti-inflammatory. Indicate in the structure the functional group that will be attacked together with the reagent (chemical formula) that attacks you from the following reagent list. There can be more than one reagent that attacks the same functional group. NOT DRAW THE PRODUCT TO BE FORMED.
what is the 1UPAC Neme tos the fullwing Malecole? OH 1. 8-Ethyl- S-hydronyhexenal 2. 3- E thylhenanal - 3-01 g 4- E thyl -2-hydroxyhevanal 4- Ethyl-2-hydroxpentamel 5. Nave of these
What is the functional group of the major organic product of the reaction below? LIAIHA H₂C ketone nitrile amine amide
There are more answers than shown in the photo.
Esters and amides can both be hydrolyzed under acidic or basic conditions. Given the molecule below, choose the 3 products that it would break up into when it is hydrolyzed. A B с OH D H+, heat, H₂O E F HO OH G HO. zu Gigué OH _OH H 1+ I کمه نکنند
Hello, I do not understand these questions and I am stuck. May I get help please?? Question: Draw the MAJOR organic product(s) for the following reactions. If no reaction occurs state no reaction in the box provided
Payalben
Hi! I need help with describing the structure of this drug Flexeril also know as Cyclobenzaprine. How would you give your audience information on this structure of this drug in a powerpoint presentation? Thank you.