EBK ORGANIC CHEMISTRY-PRINT COMPANION (
4th Edition
ISBN: 9781119776741
Author: Klein
Publisher: WILEY CONS
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Draw the condensed structure of the organic molecule that produces sodium propanoate when reacted with NaOH.
Correct each molecule in the drawing area below so that it has the structure it would have if it were dissolved in a 0.1 M aqueous solution of NaOH.
If there are no changes to be made, check the No changes box under the drawing area.
No changes.
HO–CH,—CH, NH
HO—CH,
OH
C™
X
с
O
N-benzylethanamide
Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Adv
toolbars. The single bond is active by default.
DC
H 12D EXP. CONT.
Gl
·
[1]
A
ZI
CH3
H
с
N
S
CI
Br
I
P
F
The following chemical equation is for an elimination reaction, where the important atoms, groups, and bonds involved have been highlighted for you:
Η Η
CI H
DBU
?
+ H-CI
Use the information provided to predict the missing organic product and draw its structure in the drawing area below. Make sure to use the same skeletal
("line") style for the structure as the rest of the equation.
Click and drag to start drawing a
structure.
X
0:0
S
sm
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Similar questions
- The compound p-methoxybenzonitrile N-oxide, which has the formula CH3OC6H4CNO, reacts with itself to form a dimer—a molecule that consists of two p-methoxybenzonitrile N-oxide units connected to each other (CH3OC6H4CNO)2. The reaction can be represented as A + A → B or 2 A → B where A represents p-methoxybenzonitrile N-oxide and B represents the dimer, (CH3OC6H4CNO)2. For the reaction in carbon tetrachloride at 40 °C with an initial concentration of 0.011 M, these data were obtained: Determine the rate law for the reaction. Determine the rate constant. Determine the order of the reaction with respect to A.arrow_forward7. The following scheme shows the intermediates in the mechanism for the synthesis of isoamyl acetate, an ester with a characteristic banana flavor. Classify steps 1, 2, 3, and 4 as addition, elimination, substitution, or acid base reactions. lo ОН gor H2SO4 2 HO HO QH₂ H2SO4 1 .H ОН له عليه ملا 4 HO 3 لیڈ جل OH HO OH + H2O Harrow_forward5. (CH 15) Define bioaccumulation and give an example (who suffers most). Rank the following 4 compounds and their ability to bioaccumulate. cl cl CI cl cl CH4arrow_forward
- Identify the type of Reaction 2-butene + Cl2 —> 2,3-dichloropropane Select your answer. Addition: Symmetrical Addition: Unsymmetrical Eliminationarrow_forwardTwo useful organic compounds that contain Cl atoms are vinyl chloride (CH2 = CHCl) and chloroethane (CH3CH2Cl). Vinyl chloride is the starting material used to prepare poly(vinyl chloride), a plastic used in insulation, pipes, and bottles.Chloroethane (ethyl chloride) is a tica roman local anesthetic. Why is the C–Cl bond of vinyl chloride stronger than the C–Cl bond in chloroethane ?arrow_forwardWhat is the structure of this molecule using this HNMR? C7H16O2arrow_forward
- Two useful organic compounds that contain Cl atoms are vinyl chloride (CH2 = CHCl) and chloroethane (CH3CH2Cl). Vinyl chloride is the starting material used to prepare poly(vinyl chloride), a plastic used in insulation, pipes, and bottles. Chloroethane (ethyl chloride) is a tica roman local anesthetic. Why is the C–Cl bond of vinyl chloride stronger than the C–Cl bond in chloroethane ?arrow_forward13. The molecular formula of compound Y is CSH100. From its NMR spectra, determine the structure of the compound. 3H 2H 3Ha 2H wlle 3.0 2,8 2.8 2.4 2.2 2.0 1.8 1.6 1.4 1.2 1.0 0.8 0.6 PPKarrow_forwardWhat is true for this reaction? CI4(1) + 4 HCI(g) CH4(g)+ 4 Cl2{g) AHrxn 0 O AHrxn 0; ASrxn 0; ASrxn > 0arrow_forward
- Which statement about elimination reactions is true? Two σ bonds are formed. Two π bonds are broken. Two π bonds are formed. Two σ bonds are broken.arrow_forward1. True or False a. UV-Vis spectroscopy is necessary for the analysis of organic compounds because most organic compounds are colored green in the presence of an extracting solvent. (T/F) b. The spectrophotometer is able to detect and report Absorbance values of a compound based on the compound's ability to absorb radiation or emit radiation. (T/F) c. A common electronic transition for an organic compound is the electron shifting from a bonding orbital to a nonbonding orbital. (T/F)arrow_forwardThe following chemical equation is for an elimination reaction, where the important atoms, groups, and bonds involved have been highlighted for you: O-H CH, CHO-CH, H* +HO—CH, Use the information provided to predict the missing organic product and draw its structure in the drawing area below. Make sure to use the same condensed style for the structure as the rest of the equation. Click anywhere to draw the first atom of your structure. 0 öarrow_forward
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