Oraw the curved arrows for the following step (mechanism patterns). (Take it one step at a time and note the differences). :0: H-O-H R R :C: H H₂O OH OH2 Br Br H-Br :0: H-H Br H₂O :0: R OH Br H₂O

Q: Draw the products and show the mechanism for the reactions below. It there are multiple products,…

A: All the reaction are type of elimination reaction. Reagents are base and they will abstract the…

Q: step 1 :0: -H₂O H n = & H H 1 step 2 step 3 step 4 H 1 H step 5 H H products H H H-O: step 6

A:

Q: O || CH3CH2 CHCH2-C-0-H + CH3OH CH3 ECH, CHACHCHa-c-o-chot Hạo CH3

A: when a Carboxylic acid reacts with alcohol it undergo dehydration to form ester as a product

Q: Select the arrow drawing that best shows protonation of an alkene. O O ii O iii iv H-CI: H-CI: ci :…

A: Given,  The arrow drawing that best shows protonation of alkene is:

Q: Draw curved arrows for the following reaction step. Arrow-pushing Instructions NOX CH3 H3C-C+ CH3…

A: Information about the question

Q: Step 2: Draw curved arrows to give elimination. : 0 MC HC ة CH CH₂ ا H H3C CH2 mayor. CH3 H H H

A: We have to show the mechanism for curved arrows.

Q: The product of this first step is called a "tetrahedral intermediate." Click on its structure. H₂C-…

A: Organic reactions can be defined as the reactions in which organic reactants react with each other…

Q: Provide the correct IUPAC name for the compound shown here. OH

A: Since,Rule of IUPAC-1) Longest chain as parent chain.2) Numbering start from those side where more…

Q: . Identify the products of the following transformations.

A: Addition of HCl to unsymmetrical alkenes follow Markonikov's addition(negative part of attacking…

Q: OCH3 C-H C–H + H,O + ? OCH3

A:

Q: What is the product of the following two-step reaction sequence? Br2 Na CH3C=CCH3 NH3 H CH3 H2N, H3C…

A:

Q: 7-9 Predict with compound in each pair will undergo an SN1 reaction more quickly. to a te ta a) or…

A: This reaction proceeds in two steps. The first step is the removal of the leaving group to form a…

Q: 1. Name the following aldehydes and ketones: (a) O (b) CH2CH2CHO CH3CH₂CCHCH3 T CH3 "o" (d) CH3 H…

A: Hello dear rules for iupac name and detailed names are attached in pictures in both the steps...…

Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…

A: Carbonyl group has electrophilic center hence, it can give nucleophilic addition reaction to…

Q: When drawing the requested mechanism, don't forget to include all lone pair electrons and non-zero…

A: Aldol reaction is the reaction between aldehyde or ketone to form the -hydroxy aldehyde or ketone.…

Q: Can you help me part H? Which is the formula of this rule of reaction?

A: The organic compound having -COOH group is called as carboxylic acid.  the organic compound having…

Q: What reagents would be needed to produce the product shown as the major product? ОН Br A) 1. H2SO4 /…

A:

Q: mechanism and draw a labeled energy profile diagram

A:

Q: For the reaction below: 2 CH3CH₂MgBr a Draw the major organic product. **** ? ChemDoodle 1. ether 2.…

A:

Q: 5. The product(s) of the following reaction Mow CH2-CH2 excess HBr CH2 is/are: heat Od CH2 MAD (A…

A: HBr dissociate and formed H+ and Br-,where H+ act as a electrophile and Br- act as a nucleopile

Q: Give handwritten answer with explanation

A:

Q: Please use Chemdraw software to draw this mechanism.

A: Please find the mechanism below as drawn using chemdraw software:

Q: Which choice shows the correct curved arrow mechanism for the given SN2 reaction? ca OI 0 000 11 |||…

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

Q: H H;C, CH3 H3C- -CH3 OAc НОАС NEN -SO3 H H;C- N=N• SO3 CH3 proton transfer H3C -SO; H3C H Helianthin…

A:

Q: Mechanisin: Which mechanism below is depicted correctly? Pho Ph Ph :0: Ph Ph + (Ph)3P=0 + Ph HH HH…

A: The mechanisms given are,

Q: 4. Draw a mechanism of the reaction below. a) i) CH3CH=CHCHCH3 + CH3O¯ Br ii) CH3 CH3-C-CH3 + HO¯ Br…

A: i) It is an example of E2 type elimination reaction. For such elimination reaction, adjacent carbon…

Q: Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) (CH3CH(CH3)NH2) is heated with each…

A: A question based on introduction to polymer that is to be accomplished.

Q: Draw the major organic product of the following process: 1) Hg(OAc)2, CH3OH 2) NaBH4, NaOH ?

A: Oxymercuration-demercuration is a two-step organic reaction used to add a hydroxyl group (-OH) to an…

Q: For the following compund, draw a mechanism

A: To write the mechanism of the given reaction:

Q: Which reagent is the nucleophile in the esterification reaction shown below? O || C-OH Benzoic Acid…

A: Nucleophile is an electron rich species. Nucleophile contain lone pair of electrons or negative…

Q: 4. Show curved arrows that illustrate the resonance in each of the intermediates. Resonance (start…

A: Which involves identical position of electrons is called resonance.

Q: Rank the following alkyl halides in order of the rate of reactivity in an SN2 reaction (slowest to…

A: -> In SN2 reaction there is only one step in which nucleophile attack and leaving group leave…

Q: f) O || CH3CH2-C-0-H + NH3 CHO CH2-C-NH2th-o-H

A: In part F , chemical reaction takes place between (-COOH) of acid with ammonia (NH3).     Reactants…

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.