Provide the systematic name for each of the following isomeric amides with the chemical formula CH₁, NO. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick ✓-+ labels ball & stick + labels ball & stick ✓- + labels 0

Provide the systematic name for each of the following isomeric amides with the chemical formula CH₁, NO. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick ✓-+ labels ball & stick + labels ball & stick ✓- + labels 0

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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Provide the systematic name for each of the following isomeric amides with the chemical formula C6H₁1 NO. (Be sure to indicate double bond stereochemistry using (E)/(Z) notation. Indicate stereochemistry in rings with the terms cis or trans. It is not necessary to use italics in writing compound names.) ball & stick + labels N-methylpent-4-enamide An error has been detected in your answer. Check for typos, miscalculations etc. before submitting your answer. ball & stick - + labels N, 3-dimethylbut-3-enamide ball & stick + labels (2Z)-2-methylpent-2-enamide
4-chloro-3,4-dimethylnonan-1-amine On a page titled Incorrect Separation Scheme print the incorrect separation schemeprovided for your molecule on Blackboard. The top of the separation scheme shows whatother compound is mixed with your molecule. Assume for the purposes of this assignmentthat both compounds are solid at room temperature. Also assume that both compounds aresoluble in ether, except ionic compounds. The goal of the separation is the isolate each ofthe two compounds from the mixture.o Below the incorrect separation scheme write a discussion of this incorrect schemeidentifying all of the mistakes in the separation scheme. Keep in mind that therewill be more than one mistake in the scheme.o For each mistake, give a detailed, scientific explanation of why it is incorrect.
Checking my answer, there was difference with solution. (organic chemistry smith 5th ed 2.47P (d)) Solution said 'the acid base reaction between pentyne and ammonia is product way because pka of pentyne is 25, ammonia is 38 so pentyne will be deprotanted by ammonia.' but I think (and as written in the book) NH4+ is stronger acid than pentyne and acid-base reaction works when reactant is stronger acid than product conjugate acid. It isn't match that pentyne makes NH4+. who is incorrect?
(b) The activating and deactivating groups could affect the position(s) of the next incoming group(s) to the benzene ring. Based on the structure below, analyze and explain the group(s) on the benzene ring is activating or deactivating group. Then, identify the product(s) formed from the following reactions. NH, CC, CH;CH,COCI AICI, (i) NH, HNO, H,SO, (ii) H Br AICI, (iii) Page 3 of 4
6. Describe concisely a chemical test to distinguish between the following pairs of compounds. Terangkan secara ringkas ujian kimia bagi membezakan pasangan sebatian berikut. (a) Propanal and propanone (b) Phenol and benzoic acid (c) Hexan-3-one and hexan-2-one
Construct flow charts (a.k.a. flow diagrams) to show how to separate each of the following pairs ofwater insoluble compounds:a) a carboxylic acid and a neutral compound (e.g., a hydrocarbon, R-H);b) a neutral compound and an amine;c) a phenol, a carboxylic acid and an amine.
ive the structure and the correct IUPAC name for a compound that is representative of each of the following: (i) Acetal (ii) Alkoxide salt (iii) Cyanohydrin (iv) Secondary Amine (v) Tertiary Alcohol
C) a nitrile D) an amine nitrite salt DIRECTIONS: Each of the following questions or incomplete statements below is followed by four suggested answers lettered A - D. Select or choose the letters of the best answer to the question or incomplete statement. 7. An organic nitrogen compound, X, gives ammonia on warming with dilute aqueous sodium hydroxide, X could be A) ethanamide B) ethylamine C) phenylamine D) amino ethanoic acid Which one of the following reagents reacts 1. in a similar fashion with both phenylamine (C H,NH,) and ethylamine. A) Br,(aq) C) conc. HNO, D) cold HNO (aq) 2. Phenylamine (aniline) can be prepared by reducing nitrobenzene with tin and concerntrated hydrochloric acid followed by the addition of alkali and finally steam distillation. The alkali is added to; A) prevent oxidation of phenylamine. B) liberate free phenylamine from solution C) dissolve excess nitro benzene D) dissolve the phenylamine 8. Arrange the following molecules in their increasing order of base…
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n ane arther. Charge repulsion: the ethylenediamine and its salts The preferred configuration for ethylenediamine are shown below. As you can see, the preferred conformation in each case depends on the protonation state of the amine groups. NH3 NH2 NH2 H. NH3 H. H. ZHN' H. H. H. H H NH3 Build the molecules and explain how the interplay between charge repulsion and hydrogen bonding explain this behavior. 1
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(b) Draw the structural formula for each of the following compounds. Lukis formula struktur bagi setiap sebatian berikut. (i) 3-isopropyl-3,4-dimethylhexanol (ii) 2-methyl-3-phenylprop-2-enal (iii) N-ethyl-N-methylbutanamine