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![4. Show how the following synthesis could be performed. (7 points)
OH
NH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa5644016-779f-4740-bb26-bd379069d798%2F5314f138-693c-45e6-aba3-e697f656e40f%2F9a5akhi_processed.jpeg&w=3840&q=75)
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- 4. Show how the following synthesis could be performed. (9 points) Br ??? BrPlease don't provide handwritten solution ..Summarize the relationship between pKa and acid strength by completing the following sentences: a. The higher the pKa of an acid, the stronger or weaker the acid. b. The lower the pKa of an acid, the stronger or weaker the acid.
- Complete each acid-base reaction and predict whether the position of equilibrium lies toward the left or toward the right. (a) CH3CCH+CH3CH2ONa+CH3CH3OH (b) CH3CCCH2CH2OH+Na+NH2NH3(l)7. For each draw the mechanism (using arrows) and label acid, base, conjugate acid, conjugate base :0: NH3 :OH H,ö:8. Propose a synthesis.
- Arrange the given alcohols in order of reactivity in an acid catalyzed dehydration reaction. O Hold and drag to reorder Fastest = 1. Second fastest = 3. Slowest = 2. OH OH HO 1) 2) 3)2. Which carboxylic compound of each pair would you expect to be stronger acid? Indicate (a) or (b) on the box provided. (2 pts.) i. (a) (b) OH OH or Me,Ń i. (a) (b) OH (ii) OH or CF3Provide a detailed step - by-step synthesis 4. OH OH
- a) Draw all resonance forms of 3-hydroxybenzaldehyde and of the corresponding conjugate base. W hich conclusions can you draw for its acidity (pKa) in comparison to phenol?| b) Draw all resonance forms of 3-hydroxybenzaldehyde and of the corresponding conjugate base. Which conclusions can you draw for its acidity (pKa) in comparison to phenol and 3-hydroxybenzaldehyde? c) Discuss the relative acidities of 2-hydroxybenzaldehyd und 4-hydroxybenzaldehyd.Br NH₂ OH NH₂ CH3 A/RO/exception Circle the more acidic compound and determine the effect responsible for such observation using ARIO methods, or if its an exception to the rule. Please explain thanks.Devise a synthesis (3-step) N*
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