Complete the following reaction. OH CH3 B مت لو OH KMnO4 HO H2O, heat C CH3 D OH CH CH3

Q: Give the IUPAC name for each of the following compounds. TO IVO c) II b) H₂C I- I CH₂ CH₂ OH CH₂

A: IUPAC nomenclature is a process of naming organic compounds.The full form of IUPAC is International…

Q: Predict the product of this reaction. A B OC D A) Br CN D) 1. KCN 2. H30, heat B) OH CO₂H n ? NH₂…

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: H2SO4 , 1s isi CH;CH2CH2CH2CH;OH

A: The answer is given below in the image provided.

Q: Show how you can synthesize the product from the starting material (no narrative text!). Include…

A: Ethyl acetate (EtOAc) is a colorless, clear, and flammable liquid with a fruity odor. It is a common…

Q: How many of the following possible reactants will complete the reaction below? H3C ? Hz H₂ OH CrO3…

A: -> CrO3/H3O+ is oxidizing agent which can oxidize both alcohol and aldehyde to carboxylic…

Q: CH30 CHO NaB Reduci Ac

A: Sodium borohydride (NaBH4) is used as a reducing agent. It is a source of hydride ions (H-) that can…

Q: More than one reagent/reaction will be necessary to produce the product from the reactant provided.…

A: When 4-bromopentanol treated with Acetyl Chloride then HCl is removed and 4-bromo-methylpentanoate…

Q: CH3 cat. H2SO4 EtОН

A: The mechanism of 4 Methyl benzoic acid with Ethyl alcohol as follows.

Q: H,SO4, heat QH CH;COOH HCI CH3 KMNO, HCI PCI4 HBr HCI PBR3 12, NaOH

A: The Answer to the following question is-

Q: Eto Eto O Et

A: The methylene carbon has most acidic  hydrogen which is then abstracted by base.  Then aldol type…

Q: What type of reaction is shown below? Br: of H-Br (gas) CH CH + H20 Ether CHCH CH,CH O An addition O…

A: Correct answer is A substitution. -OH group is substituted by -Br group in the given reaction.

Q: What is the major product of the following reaction? OH oc | (1) BH3 (2) H₂O₂, OH-

A:

Q: Predict reagents needed to complete this E1 elimination reaction. Br

A: The formation of alkene from an alkyl halide in the present of a certain chemical reagent is called…

Q: NaOH OHO < 1. BH-THF 2.H₂O₂, NaOH) HOCH₂CH₂CH₂ OH TSOH B C D < NaOH H₂O HOCH₂CH₂CH₂OH TSOH, H₂O…

A: Organic reaction: conversion of acetal to ketone.

Q: 3. For the following reactions, determine the major product(s) and the primary mechanism giving rise…

A:

Q: Major product

A:

Q: Br KO'Bu (one equivalent) t-BuOH

A: Alkyl halides give an E2 elimination reaction with a strong base. In the E2 elimination reaction,…

Q: вх H КОН (catalytic) EtOH 78°C

A:

Q: Complete each acid-base reaction and predict whether the position of equilibrium lies toward the…

A:

Q: H Ph 1) NEt3, DMF, 40°C 2) mild H3O* workup e.s Ph OH minor product OH Ph major product

A:

Q: How doyou complete this reaction pathway H3O+

A:

Q: H Ag:0, NaOH A H;O* B H;O. A LIAIH, H;0 CH;CH,CN D Eter

A: Carbonyl compounds are the compounds, containing the C=O group. aldehydes and ketones are carbonyl…

Q: 1. Hg(OAd)z, но но 2. Na BH

A: In this reaction, an alkene is treated with mercury(II) acetate, Hg(OAc)2, and the product formed is…

Q: What is the systematic name of the product P of this chemical reaction? CH3 OH OH O | || -CH-CH-C-OH…

A: Answer:When an acid reacts with water than formation of salt and water takes place and significant…

Q: acetone H,C но H,C . OH tien is HGl OH H,C

A: The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group…

Q: Short answer questions 1) Predict the products of the following reactions. CH₂OH OH OH CH₂OCH 3 OH…

A: Step 1: Step 2: Step 3: Step 4:

Q: H3C CH,OH H,SO, CH3 H3C- H3C- H3C- H3C- OH H3C- OH H;C- OH OH 0-CH3 H3C-O -CH3 H3C-O -CH3 H3C-O A C

A:

Q: Which set of answers is organized in order from highest to lowest priority? A. –CH2NH2 > –CN > –COOH…

A:

Q: H3C NH, H h. N.

A: Ammonia or primary reacts with aldehyde or ketone to produce imine Secondary amines react with…

Q: EtO OEt + C3 and below COOH

A: The retro synthetic pathway of the desired product is shown below. In this retro synthesis process…

Q: 1) NaCN 2) dil H3O* a) H2O/H,O* b) CH3 180 °C HO H3C CH3 c) 25 °C HO (R)-2-bromobütan +

A: (1) The given reaction is: Mechanism of the given reaction: (2) The given reaction is: Mechanism…

Q: What is the final organic product formed in the reaction below? III он CH₁ H H Н но II IV H, Hg" H…

A: Alkynes when treated with water (H2O) in the presence of HgSO4 and H2SO4 undergo an electrophilic…

Q: How many of the following possible reactants will complete the reaction below? CrO3 том ? и H3C H3O+…

A:

Q: What is the product of this reaction? O а НО ОН OH 1. BH 3 THF 2. H2O2, NaOH

A:

Q: .CN Heat CN Na / CH3OH / NH3 (liquid) +

A:

Q: 5. Complete the following reactions by writing the correct product Ph H- OTs NaOCH3 H- Ph Methanol…

A:

Q: Classify the reaction below. CH₂=C=O + H₂O CH3COOH

A: Classification of reaction.

Q: O OCH₂CH3 NO₂2 H 6-7 steps 4 steps 4 steps Ph CH₂OCH3 H

A:

Q: 1. Draw the product(s) of the following reactions (a) 1. Br2, CH&OH 2. DBN 1. ВНз 2. H2O2, NaOH (b)…

A:

Q: NON H. H,N a) HC CH3 b) H,C CH,

A: Organic reaction mechanisms

Q: Complete the following reactions: a. CH,-C-0-C-CH,+ CH,-OH -→ | CH, — ОН | b. CH,CH— С-ОН + H*, heat…

A: To complete the following reaction.,

Q: 14. What is the main product of the reaction shown below? COOH COOH OH ONa A OH OH NaOH H,O COOH B…

A:

Q: For the following reactions, predict the likely product(s) of the reaction or write 'no reaction. Me…

A: Given are organic reactions. The reactions are electrophilic aromatic substitution reactions.…

Q: 16) No BHg EtoH/ HO Etott ard

A: Reduction of ester in presence of NaBH4. Gives alcohols. Correct option is C.

Q: H. Mg HC-C-I CH3 Et0

A: Magnesium metal reacts with an alkyl halide in the ether solvent to form Grignard reagent. The…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.