Name the following amine, and identify its structural type: primary, secondary or tertiary. ball & stick labels (Ignore chirality, but do specify other stereochemistry, e.g. cis and trans. It is not necessary to use italics in writing compound names.) Name: N-methyl-1-methylethanamine Structural type: secondary + wrong Submit Answer Try Another Version 2 item attempts remaining

Name the following amine, and identify its structural type: primary, secondary or tertiary. ball & stick labels (Ignore chirality, but do specify other stereochemistry, e.g. cis and trans. It is not necessary to use italics in writing compound names.) Name: N-methyl-1-methylethanamine Structural type: secondary + wrong Submit Answer Try Another Version 2 item attempts remaining

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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CHEM-240-x1-x2- X 09 KEY Stereoche X *Organic Chemist x functional groups X 08 KEY Constitutic X *Molecular Model X b Draw the lowest Course: NEUR-35 X A https://moodle.viterbo.edu/pluginfile.php/1286283/mod_resource/content/0/Molecular%20Models%20Lab%20assignment%202.. Not syncing A) Read aloud 7 Draw E Highlight O Erase 3 of 4 5. Draw (15,3R)-1-bromo-3-methylcyclohexane in its lowest energy conformation. 6. а. Draw the following molecule as a flat ring skeletal structure with correct stereochemistry. H b. Is the chair in 6a. in its lowest energy conformation? Provide your rationale. 11:31 AM O Type here to search 9. 10/5/2020 +
Please provide the IUPAC name (only) for the compound that best represents the spectroscopic data here: • Molecular formula: C4H100 Important IR data (cm 1): 3280 (broad); 2910-2950 (many); 1053 • All 'H NMR data shown as x.xx ppm (splitting), integration. 1.23 ppm (t), 3 1.23 ppm (d), 3 "-OH" 1.46 ppm (m), 2 4.03 ppm (m), 1 5. PPM
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
X + app.101edu.co H₂C CH3 CH3 H₂C F3 O 00 KⓇ 11 -CH3 CH3 IV F4 O₂N Rank the following compounds in order of increasing basicity. Q Search % 5 N V F5 E Your Aktiv Learning trial expires on 05/23/23 at 12:59 AM ||| ... 6 Ⓒ 7, OC Search F6 Question 10 of 20 LO & 7 F7 * 8 F8 F9 9 A) II < I
BENZOIC ACID(Screenshot2113) : Find Bonds, Absoprtion Peaks [cm-1] and their functional groups (Alkane/Alyne/Alchol/Arene/etc..)
Provide the correct systematic name for the compound shown here. H3C (S)- 4- Question 11 of 25 tert- NH₂ CH3 (Z)- || (R)- | (E)- 3- 6- 2- 5- di tri cyclo sec- iso hex but amino meth nitro pent Submit +
Compound K: molecular ion at 88; IR peak at 3600-3200 cm-1; 1H NMR data (ppm) at 0.9 (triplet, 3H), 1.2 (singlet, 6H), 1.5 (quartet, 2H), and 1.6 (singlet, 1H). Propose a structure.
Submissions are not permanently recorded Using the JSME editor () draw the molecule, with formula C4H30, whose 'H NMR spectrum is shown below. The guide on how to draw your structure can be found here. 6H, d 1H 1H, Septet 10 7. 6 3 2 HPM-03-176 ppm [HỊC(=0)CC=C
▼ Part C Draw the condensed structural formula for methionylglutaminyllysine at physiological pH Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. DSCQH12 EXP NN DE [1] A ADO Submit Request Answer L CONT L Marvin JS by ChemAxon DA I UZOJ - PF H.
Drawing the structure and provide the number of carbon atoms in the parent chain 1. N-benzyl-N-methylbutan-1-amine 2. (E)-5-(1-bromopropyl)-4,6-dihydroxy-3-methocy-9-oxodec-7-enal 3. 3-methoxy-2-methyl-5-methylenexyclohexanol 4. 2-amino-N-(2-carboxyphenyl)-4-chlorobenzoic acid 5. (Z)-3-(4-hydroxyphenyl)prop-2-enoic acid 6. 3,4,5-trimethylbenzamide 7. 2-(1-chloromethyl)benzoyl chloride 8. ethyl 3-(4-methoxyphenyl)-3-oxopropanoate
2.(a) Consider the isomers shown below. 100 50 BL 41 51 65 77 L 0 100 50 Br 0 1-Bromo-4-propylbenzene 41 51 63 91 77 117 thi lam سل....ال Sample B Bustosala 90 103 119 und suchtelia 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 m/z (3-Bromopropyl)benzene Sample A 103 al h 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200 210 m/z Br ii) Draw the structure of the base peak ion for each sample. 198 J.J. 156 169 198 190 200 i) Using the mass spectra, determine which sample is 1-bromo-4-propylbenzene and which is (3- bromopropyl)benzene.
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