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(a)
Interpretation:
From the given acid derivative pair which compound undergoes hydrolysis faster is to be determined.
Concept introduction:
If the carbonyl group is attached to the electron withdrawing group like
If the carbonyl group is attached to the electron donating group like
(b)
Interpretation:
From the given acid derivative pair which compound undergoes hydrolysis faster is to be determined.
Concept introduction:
If the carbonyl group is stabilized by the resonance then it is less reactive. So in this case rate of hydrolysis of acid derivative is slower.
If the carbonyl group is less stabilized by the resonance then it is more reactive. So in this case rate of hydrolysis of acid derivative is faster.
(c)
Interpretation:
From the given acid derivative pair which compound undergoes hydrolysis faster is to be determined.
Concept introduction:
As the number of
If the carbonyl group is stabilized by the resonance then it is less reactive. So in this case rate of hydrolysis of acid derivative is slower.
If the carbonyl group is less stabilized by the resonance then it is more reactive. So in this case rate of hydrolysis of acid derivative is faster.
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Chapter 21 Solutions
Organic Chemistry: Principles And Mechanisms
- 9: Complete the missing entities for following reactions (e.g., major product(s), reactants, and/or solvents) for the SN2 reactions to occur efficiently. Include curved-arrow mechanism for reactions a) to d).arrow_forwardComplete the missing entities for following reactions (e.g., major product(s), reactants, and/or solvents) for the SN2 reactions to occur efficiently. Include curved-arrow mechanism for reactions a) to d).arrow_forwardQUESTION 3: Provide the synthetic steps that convert the starting material into the product (no mechanism required). HO OH NH CH3 multiple steps 요요 H3Carrow_forward
- Q6: Predict the effect of the changes given on the rate of the reaction below. CH3OH CH3Cl + NaOCH3 → CH3OCH3 + NaCl a) Change the substrate from CH3CI to CH31: b) Change the nucleophile from NaOCH 3 to NaSCH3: c) Change the substrate from CH3CI to (CH3)2CHCI: d) Change the solvent from CH3OH to DMSO.arrow_forwardQ3: Arrange each group of compounds from fastest SN2 reaction rate to slowest SN2 reaction rate. a) CI Cl فيكم H3C-Cl A B C D Br Br b) A B C Br H3C-Br Darrow_forwardQ2: Group these solvents into either protic solvents or aprotic solvents. Acetonitrile (CH3CN), H₂O, Acetic acid (CH3COOH), Acetone (CH3COCH3), CH3CH2OH, DMSO (CH3SOCH3), DMF (HCON(CH3)2), CH3OHarrow_forward
- Suppose the rate of evaporation in a hot, dry region is 1.76 meters per year, and the seawater there has a salinity of 35 ‰. Assuming a 93% yield, how much salt (NaCl) can be harvested each year from 1 km2 of solar evaporation ponds that use this seawater as a source?arrow_forwardhelparrow_forwardExplain why only the lone pairs on the central atom are taken into consideration when predicting molecular shapearrow_forward
- (ME EX1) Prblm #9/10 Can you explain in detail (step by step) I'm so confused with these problems. For turmber 13 can u turn them into lewis dot structures so I can better understand because, and then as well explain the resonance structure part. Thanks for the help.arrow_forwardProblems 19 and 20: (ME EX1) Can you please explain the following in detail? I'm having trouble understanding them. Both problems are difficult for me to explain in detail, so please include the drawings and answers.arrow_forward(ME EX1) Prblm #4-11 Can you please help me and explain these I'm very confused in detail please. Prblm number 9 I don't understand at all (its soo confusing to me and redraw it so I can better depict it).arrow_forward
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