6. A student tried to form the iodohydrin of the alkene shown. However, they isolated an unexpected product. Propose a complete mechanism that explains the formation this product. но. مع OH P Product not found 12, H₂O OH S. D 1₂ H₂O Product found looks like

Q: Predict Products A through F in the following multi-step synthesis. Be sure to include…

A: Structure of reactant and reagent.

Q: Draw the product of the reaction shown below. OH он РСС CH2CI2

A: Here , we have to look at selectivity  of PCC (pyridinium  chlorochromate) CH2Cl2 reagent,

Q: Which of the following best describes the product(s) of this SN2 reaction? OH NaOH Br

A:

Q: Draw an alkyl halide and choose the best reaction conditions that would undergo an SN2 reaction to…

A: In organic chemistry substitution reaction are those reaction where one functional group is…

Q: С. H2SO4 OH

A:

Q: OH H₂SO4 1-cyclohexylethan-1-ol 1-ethylcyclohex-1-ene

A: The reaction between alcohol and sulfuric acid is an example of elimination with hydride shift.

Q: H. O N Br A E

A: The given reaction is an example of [4+2] diel's alder reaction that take place between diene and…

Q: HCI MEOH a)

A: Since you have posted a question with multiple sub- parts, we will solve first three sub- parts for…

Q: 1) CH,SH 2) Н, о*

A:

Q: A student attempted to brominate the double bond in pent-4-en-1-ol, but ended up with the following…

A: The nucleophilic substitution reaction involves the attack of the nucleophile on the carbon bonded…

Q: Draw the steps to produce the product. reagents can have up to 4 carbons

A: The reaction steps are as follows:Step (i) Reductive amination of a ketone with ammonia in the…

Q: Draw the structure of the major organic product of the following reaction. Predict whether the…

A: The given reaction is Aldol reaction. In this reaction when two moiety of aldehyde or ketone (…

Q: с. НО, d. НО НО. НО ОН ОН CH₂OH ОН CH₂OH ОН HCI CH3CH₂OH HCI ОН

A: Glucoside formation involves the attachment of a glucose molecule to another compound, resulting in…

Q: What will happen if the shown hydrogenation reaction is done using Lindlar's catalyst? H2 F it will…

A: Hydrogenation is the process of addition of H2 across carbon-carbon double bond/triple bond. The…

Q: Propose a mechanism for the following reaction. Include curved arrows to show MeO2C CO₂Me 1) 1…

A:

Q: Below is one of the reactions used in the synthesis of lopinavir. What type of reaction is this? H…

A: In the given transformation NaOH is acting as a base and THF is solvent.

Q: Br CI НО О ОН ОН SCH3 ОН

A: Given are organic reactions. Note: According to Bartleby Q&A guidelines we are supposed to…

Q: predict the products of the following substitution reactions, and specify whether each proceeds by…

A:

Q: 03, Zn/H+

A:

Q: a. CI Br NH₂ DMSO CH3 CH3CN

A: The question is based on organic reactions.     we need to identify the product formed and explain…

Q: b. H₂C H3C + H CH3 -OCH3 DMSO -OCH3 CH3OH

A:

Q: 2. The following alkene can be made using either of the two schemes below. Which pathway is better?…

A: Both these reactions are Wittig reaction. Both involves formation of ylide (species with opposite…

Q: In the Friedel Crafts reaction shown, which aromatic carbon (labeled a-d) is the most likely to end…

A: Friedel-Crafts Alkylation is to replacement of an aromatic proton with an alkyl group.

Q: 5) Circle the Markovnikov product of the acid-catalyzed hydration below. Draw the energetically…

A:

Q: Prep 1. The following is a Michael addition. Propose the product and show a mechanism consistent…

A: Michael Addition can be defined as the nucleophilic addition of a nucleophile (or a carbanion) to an…

Q: а). + H2SO4 b). Br

A: The reactions given are,

Q: LOMM H2N' H. .N. pH: 4-5 H Choose the statements that best describe this reaction. The product shown…

A:

Q: Draw the steps to produce the product. Show the intermediaries. Reagents may have up to seven…

A: Here we have to show the steps to produce the product. Given reaction is:-Here reagents may have…

Q: Propose a mechanism for this transformation. Add any remaining curved arrow(s) to complete step 1 of…

A:

Q: Show the mechanism for the nucleophilic aromatic substitution below. Br NH2 NaNH, ZON NaBr ZON

A:

Q: Which elimination product is the major product? U r U U a с e Br H₂O Heat HO a НО, b с

A: Saytzeff's rule: It predicts the regioselectivity of the alkene formed by the elimination reaction…

Q: ? Br What is the best reagent for the transformation shown above? B E „Mgl A D PPH3

A: We know that R-Li gives exclusively gives 1,2 product.

Q: 1 H3C- H3C H3C= O₂N CH3 CH3 CH3 CH3 [1] 03 [2] Me₂S [1] BH3 [2] H₂O2, HO H₂O H₂SO4 Cl₂ AICI3

A: Given,

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.