5.compound?ABCDEA.2,3-dimethylbutanenitrilea,ß-dimethylbutyrnitrileB,y-dimethylbutyrnitrileD. 3,4-dimethylbutanenitrileE. 3,4-dimethylpentanenitrileC.What is the IUPAC name for the following 6.ABCDE7. Rank the following carboxylic acid derivatives indecreasing order (most to least) of reactivity towardsnucleophilic substitution.CNB.||NH₂A. | > |V > III > II >VIV > | > ||| > II >VC. | > ||| > || > |V >VIII > IV >V > I|>|IV >V > > III > ||IVCIVeO Naphenyl-N-propyl-2,3-dimethylbutanamide?ان فن هےB.C.D.E.اني ف ن ه هB.Provide the structure for N-D.8. Predict the product for thefollowing reaction.E.===>>III===>>mthemoOCIOH SOCI₂pyridineIVOH||SO₂CIOH

Answered: Image /qna-images/answer/c89a1dd8-ad90-4cff-a9d0-a6bd4b562e4d.jpg

What is the IUPAC name for the following 6. compound? 5. ABCDE A. B. C. E. CN 2,3-dimethylbutanenitrile a,ß-dimethylbutyrnitrile B,y-dimethylbutyrnitrile 3,4-dimethylbutanenitrile 3,4-dimethylpentanenitrile phenyl-N-propyl-2,3- dimethylbutanamide? ABCDE A. D. Provide the structure for N- E. my m the the tomo ===>>

What is the IUPAC name for the following 6. compound? 5. ABCDE A. B. C. E. CN 2,3-dimethylbutanenitrile a,ß-dimethylbutyrnitrile B,y-dimethylbutyrnitrile 3,4-dimethylbutanenitrile 3,4-dimethylpentanenitrile phenyl-N-propyl-2,3- dimethylbutanamide? ABCDE A. D. Provide the structure for N- E. my m the the tomo ===>>

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...

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Ofa/?tstamp3D1651674579 PART 1: TRUE OR FALSE. Choose A If the statement is true. Otherwise, choose D. 1. The carbocation of n-propyl alcohol is more stable than the carbocation of isopropyl alcohol. 2. The C-0-C bonds in ether have a higher bond dipole than the C-0-H bond in alcohol. B. When n-propyl alcohol undergoes an elimination reaction, the resulting product is an alkene. 4. As the alkyl chain increases in molecular weight among primary alcohol, the solubility in water increases. 5. An ethoxide ion exhibits greater proton-accepting property compared to an ethyloxonium ion. 5. Phenol is more acidic than cyclohexyl alcohol due to the electron-donating ability of phenolic oxygen. 7. When isopropyl alcohol reacts with HCI, the resulting product is 2-chloropropane. B. Nucleophilic molecules are electron-rich molecules that can "attack" electron-deficient molecules. 9. Based on the physical property, hydroquinone has a lower boiling point compared to catechol. 10. When FeCla is used…
Questions 17 and 18
CH3 :Q: CH3-CH-C-OH For the compound: a. Circle the 2 polar groups in the structure above. b. Does this compound have a higher or lower bp than an aldehyde? Is this compound more or less soluble (in water) than an ester? C.
19. Which of the following best describes the molecule shown below? H. CH3 N. A. Secondary amine 8. Methylaminocyclohexane C. Cyclocarboxylic acid D. A cycloalkane
10.2 Provide names for the compounds. NO2 GH3 CH,CH2CH3 Br C. b. a.
Which of the following is a para-substituted compound?
Draw the structure corresponding to each IUPAC name (specifically, D-F please)
II. Draw the structures corresponding to each name. 1. m-bromoaniline 2. p-bromotoluene 3. 1-chloro-3,5-dimethylbenzene 4. O-iodophenol 5. 1,3,5-trichlorobenzene 6. O-hydroxybenzenesulfunic acid
1. What is the product of the reaction? 1) LAH 2) Hо* но OH а. b. OH с. HO. HO. d. 2. Which amine is expected to be least soluble in HzO? `NH2 а. c. N. b. d. ZI
give the following structure (condensed or detailed structural formula), name, properties, and uses of 1 compound that belongs to the class a. diazo b. Hydrazino
9. Which compounds react together to form an ester? CH3CH₂OH CH3CH₂COOH II. CH3CH CHO IV. CH3CH₂COCH3 I. III. I and IV only II and III only I and III only D) Both I and II and I and IV would produce esters. A) B) C)
1. What is the correct IUPAC name for the following compound? H. N. QA Diphenylamine O'B. 1,1 diphenylamine OCN,N-diphenylamine O D. None of the above is correct