EBK FOUNDATIONS OF COLLEGE CHEMISTRY
15th Edition
ISBN: 9781119227946
Author: Willard
Publisher: VST
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Chapter 6, Problem 39AE
Interpretation Introduction
Interpretation:
The formula for the compounds that ferricyanide would form with the cations of elements
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Draw the major organic product when each of the bellow reagents is added to 3,3-dimethylbutere.
✓ 3rd attempt
Part 1 (0.3 point)
H.C
CH
CH
+
1. BHG THF
210 NaOH
NJ
10000
Part 2 (0.3 point)
HC-
CH
HC
2741
OH
a
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1. He|DA HO
2. NIBH
さ
士
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j = uz C
H
F
F
box
Synthesis of 2-metilbenzimidazol from 1,2-diaminobenceno y propanona.
Predict the product of the following reaction.
1st attempt
HI
1
product
50300
Jul See Periodic Table
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P
Br
石尚
I
Chapter 6 Solutions
EBK FOUNDATIONS OF COLLEGE CHEMISTRY
Ch. 6.2 - Prob. 6.1PCh. 6.3 - Prob. 6.2PCh. 6.4 - Prob. 6.3PCh. 6.4 - Prob. 6.4PCh. 6.4 - Prob. 6.5PCh. 6.4 - Prob. 6.6PCh. 6.4 - Prob. 6.7PCh. 6.5 - Prob. 6.8PCh. 6.5 - Prob. 6.9PCh. 6.6 - Prob. 6.10P
Ch. 6.6 - Prob. 6.11PCh. 6 - Prob. 1RQCh. 6 - Prob. 2RQCh. 6 - Prob. 3RQCh. 6 - Prob. 4RQCh. 6 - Prob. 5RQCh. 6 - Prob. 6RQCh. 6 - Prob. 7RQCh. 6 - Prob. 8RQCh. 6 - Prob. 9RQCh. 6 - Prob. 10RQCh. 6 - Prob. 11RQCh. 6 - Prob. 12RQCh. 6 - Prob. 1PECh. 6 - Prob. 2PECh. 6 - Prob. 3PECh. 6 - Prob. 4PECh. 6 - Prob. 5PECh. 6 - Prob. 6PECh. 6 - Prob. 7PECh. 6 - Prob. 8PECh. 6 - Prob. 9PECh. 6 - Prob. 10PECh. 6 - Prob. 11PECh. 6 - Prob. 12PECh. 6 - Prob. 13PECh. 6 - Prob. 14PECh. 6 - Prob. 15PECh. 6 - Prob. 16PECh. 6 - Prob. 17PECh. 6 - Prob. 18PECh. 6 - Prob. 19PECh. 6 - Prob. 20PECh. 6 - Prob. 21PECh. 6 - Prob. 22PECh. 6 - Prob. 23PECh. 6 - Prob. 24PECh. 6 - Prob. 25PECh. 6 - Prob. 26PECh. 6 - Prob. 27PECh. 6 - Prob. 28PECh. 6 - Prob. 29AECh. 6 - Prob. 30AECh. 6 - Prob. 31AECh. 6 - Prob. 32AECh. 6 - Prob. 33AECh. 6 - Prob. 34AECh. 6 - Prob. 35AECh. 6 - Prob. 36AECh. 6 - Prob. 37AECh. 6 - Prob. 38AECh. 6 - Prob. 39AECh. 6 - Prob. 40AECh. 6 - Prob. 41AECh. 6 - Prob. 42AECh. 6 - Prob. 44CE
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- Indicate the substitutes in one place, if they are a diazonio room.arrow_forwardIndicate the product formed in each reaction. If the product exhibits tautomerism, draw the tautomeric structure. a) о + CH3-NH-NH2 CO2C2H5 b) + CoH5-NH-NH2 OC2H5arrow_forwardIndicate the formula of the compound, that is the result of the N- alquilación (nucleofílic substitution), in which an additional lateral chain was formed (NH-CH2-COOMe). F3C. CF3 NH NH2 Br о OMe K2CO3, DABCO, DMFarrow_forward
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