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Q: = HA = H,O* = A %3D The strongest acid is: А. НХ В. HY С. HZ D. Not enough info HX HY HZ
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A: Bronsted-Lowry acid-base theory: The Bronsted-Lowry acid-base theory states that the acid is a…
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A: Acid and base play an important role in chemistry. In organic chemistry they are very useful.
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Q: Rank the following compounds in order of increasing acidity.
A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…
Q: b) Rank the following in order of increasing acidity. H3C HS. Но OH A. В 오
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Q: 2.51 Rank the compounds in each group in order of increasing acidity. a. b. C. OH CI CI NH2 OH OH SH…
A: Acidity of a compound means how easily a compound release hydrogen ions. Organic compounds are the…
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A: The compounds given are,
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Q: c) Rank the following compounds in order of decreasing acidity. CO 2H CO2H
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Q: `NH2 но, -OH -NH2
A: The following reaction is known as amide formation reaction.
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A: The main reason is explained below:
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A: Carboxylic acids are more acidic than alcohols or phenols, although all of them have a hydrogen atom…
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A: Major product
Q: 2) Rank the Acidity of the following sets of compounds. b) c) CICH, ; a,CH, ; ca. ; a,CH COOH
A: As you not specified so I am giving answer of first three question as per guidlines Acidity is…
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Q: AA RANK ACI, STRONGEST 0tHE WEAKEST B)EX8IAINTHE 6TRONGER Ačio [R]
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Q: cts for the fouwing reactions: .? HBr ROOR HBr (a) (b) HOI HBr (c) :? HBr ROOR
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A:
Q: 3. Arrange the following compounds in order of INCREASING acidity (starting with the least acidic)…
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Q: Which compound is a stronger acid in each pair and why? OH OH vs. vs. CN ZI
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A: This reaction is known as Edman degradation. In this process the amino-terminal residue is cleaved…
Q: edict the product of the following reaction: 1) Na OF+ 2) H3O+ ?
A: In this question we have to tell the product of the reaction.
Q: (A) → H H (C) Which indicated hydrogen is most acidic? CH3 (D) (B) –→ H O D B
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A: Part a- The first compound is an alcohol, the second compound is an amine and the third compound is…
Q: 2A. Rank the following compounds with increasing acidity: (1 = least acidic; 3 = most acidic) (a) Me…
A: the solution is as follows:
What are the parts for d,e,f
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- Predict the major products formed when 2- methyl-1-butene reacts with: H2, Pt/25°C. Show the reaction mechanism the given alkene reactionsPredict the major product(s) and provide a mechanism for the reaction below. Includestereochemistry.Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)
- Tributyltin hydride (Bu3SnH) is used synthetically to reduce alkyl halides, replacing a halogen atom with hydrogen. Free-radical initiators promote this reaction, and free-radical inhibitors are known to slow or stop it. Your job is todevelop a mechanism,When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.What is the expected product of the reaction scheme below?
- Rank the species below in order of increasing nucleophilicity in protic solvent. I. H2O II. CH3S— III. CH3COO— IV. t-BuO— I, II, IV, III I, III, II, IV I, III, IV, II I, II, III, IVAromatic iodination can be carried out with a number of reagents, including iodine monochloride, ICl. What is the direction of polarization of ICl? Propose a mechanism for the iodination of an aromatic ring with ICl.1. Write equations, using displayed formulae, to show the conversion of but-1-eneinto:a) polybut-1-eneb) 1,2-dibromobutane 2. a) Explain why alkenes tend to react with electrophiles.b) Show the mechanisms for the following reactions:i) ethene with bromineii) but-2-ene with hydrogen bromidec) Explain how bromine can behave as an electrophile. 3. Reaction of but-1-ene with HBr gives two products in unequal amounts. In eachcase, identify the two products, state which is the major product, explain why it isthe major product and give the mechanism for its formation.
- LDA/THF, 78°Clongrightarrow Predict the major product of the following a- halogenation/a - alkylation reactions under the given reaction conditions.Need help ASAP pls & thank you! "Provide the stable organic product(s) for the reactions below."I’m currently trying to write a lab report for the synthesis of dimolybdenum tetraacetate [Mo2(O2CCH3)4] from the reaction of molybdenum hexacarbonyl, Mo(CO)6 in glacial acetic acid and acetic anhydride under a nitrogen atmosphere, involving the difficult formation of a quadruple bond and requires high heat and long reaction time (approximately 20 hours). But these are the question I’m stumped on: 1. Why need the reaction be done under nitrogen? We also added dichlorobenzene and hexanes during the reaction. 2. Explain the purpose of dichlorobenzene and hexanes. 3. Why does the reaction take 20 hrs?