In the window below, draw the form of the alkyne that will predominate at equllCH3 CH, CH, C=CH + NaOCH, CH3? + Conjugate acid of the baseAcidpKaAcidpKCH3 CH351H2O15.7NH338CH3 NH3+10.64H235H2CO310.33HC=CH+NH4259.24CH3 CH2 OH15.9 H30+-1.74• Do not include counter-ions, e.g., Na", I, in your answer.| の

Answered: Image /qna-images/answer/6902d401-bb9d-45ba-a9f6-635d1a5708d5.jpg

In the window below, draw the form of the alkyne that will predominate at equlllb CH3 CH, CH, C=CH NaOCH, CH3 = ?+Conjugate acid of the base pka pK Acid Acid CH; CH3 51 H20 15.7 NH3 CH3 NH3 + 38 10.64 H2 35 H2CO3 10.33 HC=CH 25 +NH, 9.24 CH3 CH2 OH 15.9 H30+ -1.74 • Do not include counter-ions, e.g., Na, I, in your answer.

In the window below, draw the form of the alkyne that will predominate at equlllb CH3 CH, CH, C=CH NaOCH, CH3 = ?+Conjugate acid of the base pka pK Acid Acid CH; CH3 51 H20 15.7 NH3 CH3 NH3 + 38 10.64 H2 35 H2CO3 10.33 HC=CH 25 +NH, 9.24 CH3 CH2 OH 15.9 H30+ -1.74 • Do not include counter-ions, e.g., Na, I, in your answer.

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

Choose the BEST classification for each structure shown below. Classifications to Choose from: Alkane, Alkene, Alkyne, Aromatic, Organic Halide (Alkyl Halide), Ketone, Aldehyde, Carboxylic Acid, Ether, Ester, Amine, Amide, Alcohol, Nitrile. CH3 CH3-CH2-CH2-CH2-CH2-CH3 CH2. CH-CEN нн H H-C-C-O-C-H нн ОН CH2 Structure 1 Structure 2 Structure 3 Structure 4 NH2 CH3 .CH3 `CH2 `CH H. CH3 „CH CH3 CH3 `CH2 CH2 ČH3 Structure 7 Structure 5 Structure 6 Structure 8 H CH;-C-Ņ-CH3 CH2-CH2-CH3 CH2 CH3 F Structure 9 Structure 10 Structure 11 Structure 12
Cheto
PLEASE ANSWER ASAP
-COH (acid) &H (aldehyde) Ar-H (aromatic) (C=C-H, vinylic OH (alcohol or phenol) X-C-H (X= halogen or oxygen) Ar-C-H (benzylic) CH 10.0 (C-C-C-H, allylic H on saturated C, base position 9.0 8.0 44 7.0 4.3 30 20 10 0 6.0 In this ¹H NMR spectrum the blue floating peaks are enlargements of the peaks to their right. 4.2 ppm Hz 5.0 1 4.0 10-13 9-10 3.0 6-8.5 4.6-5.7) 1-5 3-4.5 2-2.7 2-2.7 1.6-1.9) .8-1.6 l 1.75 1.70 1.65 2.0 1.0 0.0 Which compound is most likely to have given rise to this spectrum?
estion 12 of 33 Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: 0 CH2-0-C-(CH2)16-CH3 о о O= = = CH-O-C-(CH2)4-CH=CH-CH2-CH=CH-CH2-CH=CH-(CH2)4-CH3 Separate each name with a comma. You will find useful information in the ALEKS Data resource. Question 13 of 33 Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH₂-01 CH-O ང CH₂-01 Separate each name with a comma. You will find useful information in the ALEKS Data resource. Question 14 of 33 Draw the skeletal ("line") structure of the triacylglycerol that could be formed from lauric acid.
Complete the following reaction. A C-NH2 B LiAlH4 ether -CH2NH2 C -NH2 D -OH
None
Pls tell if each reaction is addition, elimination, condensation, substitution, onxidation, reduction. Pls help on all three ASAP
Name the compounds in the photo Please name 3,7,9,10,11 like they are named in 4 and 8 and the structures also with their common names