Propose a reasonable and detailed mechanism for the following transformation: S cat. H₂PO, EtOH OH × Incorrect. Write the mechanism for step one of this reaction. Show lone pairs and formal charges. Only the acidic hydrogen should be drawn out with a covalent bond. Show stereochemistry on reactants and products. H P-OH སྣ་ དེ་དག་་ཚེ་ད་ག OH Edit Drawing OH

Q: PQ-12. What is the major product of this reaction? 1) LiAlH4, Et₂O 2) H3O+ OH (D) OH (A) H (B) HO

A: Reduction of ester with LiAlH4.LiAlH4 is a strong reducing agent which is used to reduce esters.

Q: QII: Starting from toluene as the only organic reagent you have and use any other inorganic reagents…

A: The ortho, para directing nature of toluene would result from substitution reaction using CH3Cl in…

Q: o N 1. LiAlH 2. H₂O 4 NH 2

A:

Q: First Writedown which reaction it is? SN1, SN2, E1? Write a stepwise mechanism for the following…

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

Q: What is the major product of the following reactions? Br NaCN 1) CH,NH, -78°C 2) NABH,

A: NaCN act as a nucleophile.

Q: Ph Ph-P: Ph Ph XL ? H H Modify the given copy of the starting aldehyde to draw the major product. Be…

A: This reaction is wittig reaction because ylide compound react with carbonyl compound to form an…

Q: Write a balanced equation to form sodium methoxide from methanol.  Choose a reactant that is strong…

A: Since methanol, CH3OH is a very weak acid, we need a very strong base like sodium amide, NaNH2.

Q: None

A:

Q: Draw the bond-line formula of the cationic organic product formed when 4-methoxyaniline reacts with…

A: Let's go through the reaction step by step and then I'll provide the structure of the…

Q: Show how the following syntheses can be achieved in as few steps as possible OH b. (Hint: Keep track…

A:

Q: Write a mechanism for the following reaction. You MUST use curved arrows to represent electron…

A: In this question, we will write the reaction mechanisms for both products by using curved arrows.…

Q: A vicinal diol has OH groups on adjacent carbons. The dehydration of a vicinal diol is accompanied…

A: Please find below the reaction mechanism:

Q: In essence, what I'm asking is, can we make a primary carbocation if it is next to a double bond…

A: A question based on reaction intermediates. Based on the stability of the carbocation, the given…

Q: What is the final product? Click on a letter A through D to answer. NHOH HA H HO 0-NH2 0-NH, N-OH…

A: This is simple process of Protonation, where H+ attacks on election rich species. In this reaction,…

Q: Choose the reaction conditions to complete the acid-base reaction shown. H C:O Q B NaNha hexane…

A: The reaction of a terminal alkyne with NaNH2 (sodium amide) in hexane is often employed in organic…

Q: Show how 1-propanol can be converted into the following compounds by means of a sulfonate ester:

A:

Q: Give the major product(s) of the following reaction. NaCN H+ ?

A:

Q: 1. Propose a mechanism to account for the formation of 2,3-dimethyl-2-butene from 3,3-…

A: We have been asked to propose a mechanism for the formation of (a) 2,3-dimethyl-2-butene from…

Q: Help with question #8

A: The correct reagent to carry out the reaction is reagent-C. The reaction has explained with proper…

Q: Devise a synthesis to prepare 1-butyne from acetylene and ethanol. + HO Complete the following…

A: At first presence of sodium amide ,it abstract acidic acetylinic  proton from acetylene molecule,…

Q: Show reagents and experimental conditions you might use to convert propyne into each product. (Some…

A: Given: Conversion of propyne into the given product.

Q: Devise a synthesis to prepare the product from the given starting material. CHI Complete the…

A: The required reagent(s) for part 1:Given that CH₃I (methyl iodide) is being converted into compound…

Q: Consider the reaction sequence below to answer the following questions: Hg(OAc)2, H₂O/THE لی ستی OH…

A: Reaction mechanism for the oxymercuration demercuration reaction.

Q: NO2 2. Starting from only cyclohexane as the sole carbon source, synthesize the ether below.

A: We have find out mechanism. Note -as per our company guidelines we are supposed to answer only first…

Q: predict the product. make sure to draw the products

A: Given are organic reactions. The given reactions are condensation reactions. The starting compounds…

Q: What is true about the reaction below? 1) Sia BH 2) H202/ OH O This is a Hydroboration-Oxidation…

A: The given reaction is Anti-Markonikov addition.

Q: The reaction shown below does not give the product indicated. Which of the following best explains…

A: Addition of hydrogen to a carbon - carbon double bond is called hydrogenation.-> Alkenes can be…

Q: 4-pyranone will readily undergo an acid-base reaction. Identify the reaction conditions that will…

A: The given reaction is shown below.We have to predict the product of the given reaction.

Q: Compound X has molecular formula C7H14. Hydrogenation of compound X produces 2,4-dimethylpentane.…

A:

Q: Two cations are possible when 1-butene reacts with acid and water. When 1-butyne reacts with H+ two…

A: In reaction with water in presence of acid, the alkyne forms carbocation which can rearrange to…

Q: 0 Give the major organic product for the following reaction. CHO H -OH HO -H H₂O 2 H -OH H -OH 0…

A: The given reaction represents the dehydration of glucose (C₆H₁₂O₆) under acidic conditions. Glucose…

Q: Predict the product(s) for the following reaction, using as much acid and water as necessary: CH—NH…

A:

Q: An unknown acid with a Keq of 14.78 yields the following products: [ H3O*] = 1.7 E1 and [ anion - ]…

A: In a chemical reaction when change in concentration of reactant and product will remain constant…

Q: An organic chemist reacts (S)-2-butanol with PBr3 in pyridine, removes the major organic product,…

A: The above reaction is proceed by SN2 mechanism in which attack of -OCH3  is done in back side of OH.…

Q: Select the best reaction conditions and reagents to perform the reaction below. D x CH3 CH₂ OH, H+…

A:

Q: Compound A, C 10H 18O, undergoes reaction with dilute H 2SO 4 at 50 °C to yield a mixture of two…

A: The organic compound can be nucleophilic (rich in electron density), or electrophilic…

Q: Compound 1 can be prepared from acetylene: H―=H The transformation above can be performed with some…

A: The objective of the question is to identify the correct reagents and their order to transform…

Q: H3CH₂C- EC-H 1. NaNH, 2. PhCHO 3. H₂O

A: This is simple problem of reaction mechanism where at first acidic proton is abstracted by the base…

Q: Draw a structure for the following compound: 2-Heptyne Draw a structure for the following compound:…

A:

Q: Give the reagent(s) AND reaction type you would use to prepare the following target molecule.

A:

Q: Several diamines are building blocks for the synthesis of pharmaceuticals and agro- chemicals. Show…

A:

Q: A vicinal diol has OH groups on adjacent carbons. The dehydration of a vicinal diol is accompanied…

A: Please find below the reaction mechanism

Q: Answer from left to right.

A: Chemical nomenclature of organic compound uses IUPAC nomenclature rules to name organic molecules.…

Q: Show reaekson and don't use hend raiting and step by step solutions please

A: Step 1:Nucleophilic Substitution (S(_N)2 Reaction):Identify the electrophilic carbon (the one…

Q: Show the reagents for the conversion below: COOH HO NO2

A: The conversion given is,