5 Draw all products of the following reaction and show the mechanism by drawing the intermediate(s) that gets formed. Label the major and minor products and show the stereochemistry if applicable. Br. CH3OH Heat

Q: 1) NaBH,/ CH,0н 2) H2O HN

A:

Q: 10) Name the reaction and draw the product (do not draw the mechanism): NaOH, NaOCI CH,

A: The complete reaction has been given in the following step.

Q: 6. Draw out the mechanism of the final step(s) of each reaction scheme (i.e., mechanism that starts…

A: The explanation is given below-

Q: NaOH 12 excess

A: The given reaction is a haloform reaction where methyl ketone reacts with iodine, bromine or…

Q: Draw the products of the attached reaction, and include the mechanismshowing how each product is…

A: Here tertiary alkyl halide is given. Methanol is a weak base and also acts as nucleophile. Tertiary…

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: Draw the products of the two step reaction sequence shown below. Use dash and/or wedge bonds to…

A: In this question, we have to draw the product of the step reaction sequence.

Q: OH ONLY CI

A: See synthesis below.

Q: 4. Please provide the structure of the product for each of the following reactions 1. CH,MgBr 2.…

A: In the Question ( 4 ) we will Identify the structure of the products in each Reaction. Then in…

Q: HCI

A:

Q: Fill in the product, starting material, or reagent for each reaction. "No reaction" is a…

A: CH3ONa is a good nucleophile which attack on less substituted carbon show below.

Q: 45. Which reagent conditions is best suited to convert the substrate into the alkene product that is…

A: Option: B If 1-Bromo-1-methylcyclohexane is treated with Sodium tert butoxide, Minor product…

Q: Select the correct statement about the reaction below. CI НО -ОН O a. The reaction is called…

A:

Q: 1. Draw the structure of the intermediate products in the following reactions: (CH)Þ-CH CH3 AICI, ?…

A:

Q: 3. Show the reaction mechanism for the following multistep transformations. Show all reagents and…

A: Alcohol is converted to bromide by PBr3 and then it is converted to Grignard reagent and that reacts…

Q: HBr excess

A:

Q: 4. In each blank, put the type of mechanism that the reaction will use to get to the product (you…

A:

Q: 3. Draw the complete mechanism and the products for each of the following SN1 reaction paying close…

A: SN1 Reaction: it is a nucleophilic substitution reaction in which the rate determining step depends…

Q: Draw the product of the reaction shown below. HO РСС CH2CI2 FF nny

A: Reaction of alcohol with PCC is the oxidation of alcohol.

Q: Identify the nucleophile and leaving group and draw the products of attached substitution reaction.

A: Nucleophiles are electron-rich species that attack the electron-deficient atom. In Heterolytic bond…

Q: Add curved arrow(s) to draw step 2 of the mechanism. Modify the given drawing of the product as…

A: In an organic reaction mechanism, a curved arrow represents the transfer of electrons. In an organic…

Q: Draw the complete mechanism of the ring opening of the epoxide below with methanol under both acidic…

A:

Q: 3. For each of the reactions a. Complete the reaction, showing the mechanism by using arrows, b.…

A:

Q: 4. a) Show the reaction mechanism for the following multistep transformations. Show all reagents and…

A: Details mechanism involved for the synthesis of target alcohol with all intermediates are shown in…

Q: final product. b) Draw the correct first step and complete the mechanism, showing the structure of…

A: (a) The given mechanism is incorrect. The carbonyl oxygen of formaldehyde is not that much basic…

Q: Add curved arrow(s) to draw step 2 of the mechanism. Modify the given drawing of the product as…

A:

Q: 5. Show the synthesis for the following product starting with the starting material (SM) given. It…

A: The given synthesis is to be carried out with detailed mechanism. The given synthesis is, The OH-…

Q: Draw the product for the attached reactions.

A: Alkenes react with water in the presence of sulphuric acid to form alcohols. The formation of major…

Q: 1. Draw the structure of the intermediate products in the following reactions: (C,H),P-CH CH3 AICI,…

A:

Q: Part 3 out of 3 Grignard reaction: 4I CH,CHO MgBr edit structure Draw the intermediate product…

A:

Q: H3O*

A: The given is the acid-catalyzed hydrolysis of alkene. The first step is the nucleophilic attack of…

Q: What is the structure of an intermediate in the methyl shift rearrangement reaction shown in the…

A:

Q: Using curved-arrow notation, draw out the mechanism for the following reaction. Be sure to include…

A: Alkenes are electron-rich species. They easily undergo an addition reaction in the presence of Br2.…

Q: Br CH3OH Нeat

A:

Q: Draw the substitution product(s) of the following reaction and show the mechanism by drawing the…

A: The products are

Q: Determine the mechanism of nucleophilic substitution of attached reactionand draw the products,…

A: The given reactant is secondary alkyl iodide and acetic acid is weak nucleophile. Thus, the…

Q: 3. Oxidation of Alcohols Mechanism: Draw the major product for the oxidation reaction below in the…

A:

Q: Draw the product of attached reaction

A: Organometallic compounds are used to increase the carbon number in the molecule. Organolithium…

Q: 5.) Please draw the products for the following reaction and draw the mechanism. HBr excess

A: Given data : Draw the mechanism  of the reactions need to be write .

Q: Draw the products of the following reaction and show the mechanism; CH3-CH2-CCH3Br-CH3 + CH3OH

A: This is the SN1 reaction .

Q: Determine the mechanism of nucleophilic substitution of attached reactionand draw the products,…

A: In the given reaction, the SN1 nucleophilic substitution reaction will occur. The first step…

Q: Draw the product of the reaction below including stereochemistry. CH3ONA HI

A: The given reaction proceeds through the E2 elimination pathway.  Because the nature of substrate is…

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

A:

Q: 5. Classify the following reagents as either nucleophiles or electrophiles: Zn2* , CH3NH2 , HS , OH2…

A: Electrophile which loves electron or having positive charge or vacant orbital  Nucleophile which…

Q: 5. a) Indicate the necessary reagents above the reaction arrow for the following reaction and…

A: We have to indicate the necessary reagents and provide the mechanism as follows in step 2:

Q: CO2ET OH Me Ме LIAIH4 H.. Me. Me H.. Me Et20 RT Me Ме Ме

A:

Q: Determine the mechanism of nucleophilic substitution of attached reactionand draw the products,…

A: Dimethylformamide or DMF is a colorless organic liquid which is miscible with water and many organic…

Q: HỌ HO

A: The reactants given are,

Q: HO COH

A: Given reaction is : Add curved arrow(s) to draw step 3 of the mechanism. Modify the given drawing…

Q: 2. Draw the product of the propanol with HBr. Show the mechanism. 3. Show how a 1,2-shift forms a…

A: 2. Propanol react with proton and forms protonated propanol. Br- act as nucleophile gives n-propyl…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.