•+ H-O-H Draw only one curved н arrow. -н H-O: н omit H20 Н. H. +H2O Н :0—н Н 11 -О—н 0—н 1- H20 Н. o-H :ö-H Н 1L

Q: OH BrCH2 COCH, CHCHN Co,CH heat The synthesis of this morpholino derivative occurs in several steps.…

A: The details solution for this reaction is provided below in attach image.

Q: Which reaction schemes is best to give the product? HO. NO2 O The following reaction scheme: CH3…

A:

Q: X Complete the following reaction 0/3 O CH3CHCICH2COCH3, AICI3 О снзсн2сH2сосі, AICI3 CH3CHCICH2CH3,…

A: Freidal crafts reaction

Q: 10. Draw a reasonable mechanism for the following reaction (cat. = catalytic %3D amount). OH H2SO4…

A: Rearrangement of carbocations.

Q: Complete the mechanism and draw the final product for the Grignard reaction below. added acid in…

A: The complete reaction mechanism Grignard reaction in step 2.

Q: Complete the mechanism for the following reaction by adding the missing bonds, charges, nonbonding…

A: A chemical reaction mechanism represents the way to form and break the chemical bonds between…

Q: A set of three nucleophilic displacement reactions is shown below: Br Br CH3 CH3CHCH2CH2CH2CH3…

A:

Q: ix. In STEPS 9-10, a hydroxide ion causes the anhydride to break down and cleave into two products.…

A:

Q: A set of three nucleophilic displacement reactions is shown below: CH3 SOH CH3CH2CCH3 SN1 reaction…

A: The replacement of any atom or group of atoms by a nucleophile is termed as nucleophilic…

Q: Show a reasonable mechanism for how the following reaction comes about OH NaONO H30* H2N

A:

Q: OH H2SO4 (cat.) H20

A:

Q: 5. Draw a detailed arrow pushing mechanism for the following reaction. Is the rate-determining step…

A: When No carbocation is formed then reaction is SN2.if carbocation is formed then reaction is SN1

Q: لمد HO HO.

A:

Q: Q3. For the substitution reactions below, draw out the reactions as shown and answer the following…

A: Inorganic chemistry we learn about two types of substitution reaction. Unimolecular nucleophilic…

Q: In a unimolecular elimination (E1) reaction, the correct order of mechanistic steps is А.…

A: E1 Mechanism Proceeds through loss of a eaving group (LG) and  then deprotonation.

Q: /hich reaction sequence will most successfully generate the product shown belov (1) HNO3/H2SO4 (A)…

A: the solution is given below -

Q: In both examples below the reactants shown are combined to bring about a nucleophilic substitution…

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. OH LOME TSOH, H20 OMe

A:

Q: 1. For each of the following pairs of SN2 reactions, indicate which reaction occurs faster: CH;CH;Br…

A:

Q: Which of the following SN2 reactions proceeds the fastest? NaSCH3 CH3-CH2-CH2-Br DMSO NaOCH3…

A:

Q: 6:- Which of the following species is likely to behave as a nucleophile and which as an…

A: We know that an electrophile is an atom or molecule which can accept an electron pair. It can be…

Q: GUse curved arrows to show the mechanism of the step below. Make the ends of your arrows specity the…

A: Mechanism of the step Product of the reaction

Q: i) (CH3)3N: (CH3)2ö: W ii)

A:

Q: Br A Br B Br C D -Br

A: SN1 reaction The SN1 reaction is a nucleophilic substitution reaction where the rate-determining…

Q: CH3(CH2 )sBr NaOH CH3(CH2)5OH + Br + A) The rate would increase because SN2 reactions favor a polar…

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Complete the mechanism for the reaction of excess ammonia with 1-bromo-2-methylbutane by adding any…

A: Amines are the organic compounds that are formed by replacement of hydrogen from ammonia. Amines are…

Q: Circle the substances considered nucleophilic and underline those considered electrophilic OH- NH3…

A:

Q: 1. Consider each substitution reaction below. For each: 1. Label the electrophile and nucleophile,…

A:

Q: provide a reasonable mechanism for the following reaction CX НО, OH H₂SO4 (cat)

A: Basically this reaction ia used in protection of aldehyde and ketone in order to prevent the…

Q: Circle the reactant that is a nucleophile and draw the mechanism using the appropriate arrows for…

A:

Q: In both examples below the reactants shown are combined to bring about a nucleophilic substitution…

A:

Q: Identify the stronger nucleophile in each pair. a.NH3, −NH2 b.CH3NH2, CH3OH c.CH3CO2−, CH3CH2O−

A: -NH2 is a conjugate base of NH3. The amine-based compound is a stronger base than the alcohol-based…

Q: (8) Which nucleophile in cach pair will react faster in SN2 reactions? Circle one choice in cach…

A: Nucleophile donates a pair of electrons to bond with the other atom. Molecules or ions with one or…

Q: Arrow-pushing Instructions MeOH Draw curved arrows to show the movement of electrons in this step of…

A: Given reaction is :  Draw the curved arrows to show the movement of electrons in this step of the…

Q: Provide a plausible arrow pushing mechanism for the reaction below. OH OMe TSOH, H20 OMe

A: The answer is mechanism

Q: Which is the best method for carrying out the following two-step transformation (as shown in…

A:

Q: rite the mechanism for the reaction below. -OH + CH3OH

A:

Q: Which reaction schemes is best to give the product? HO. NO 2 O The following reaction scheme: CH3…

A:

Q: Which compound is a major product of the reaction sequence shown in the box? 1. EtO Na+ OEt 2. HСI,…

A:

Q: Identify the stronger nucleophile in each pair. a. NH3,−NH2 b. CH3NH2, CH3OH c. CH3CO2−, CH3CH2O−

A: Nucleophile  : Molecule which easily donates electron pair are called nuclephile.

Q: An SN1 reaction is shown in the box; the reaction profile for this reaction is shown below. Identify…

A:

Q: Consider the reaction below. [1] Draw curved arrows to show the movement of electrons in each step.…

A: #13: The reactant is a protonated alcohol and the product is an alkyl chloride.  The reaction shows…

Q: lect which molecule is the better nucleophile in e following pair: Br- or Cl- in H20 СНЗО-or CНЗОН…

A:

Q: Sn2, E2  E1cb  Sn1, E1 (anti)  E2, E1cb  Sn1, E1   2 steps poor leaving group 2 carbons…

A: Primary halides with strong nucleophiles prefer to form SN2 products. Branched halides with a strong…

Q: Select the arrow drawing that best describes this step of an E1 reaction. H I-0: І H3C I нн i 1-0:…

A:

Q: Which reaction does not correctly circle the more stable base? A) + CH3 B) + OCH3 OCH3 C) Но + H20 +…

A:

Q: 4. Circle the electrophilic and nucleophilic atoms in each substitution reaction below. Provide the…

A: We have to identify the electrophilic atom and the nucleophilic atom, also the stereochemistry of…

Q: Complete the mechanism and draw the final product for the Grignard reaction below. It is not…

A: Its an organometallic reagent used as very strong nucleophile in organic chemistry.

Q: For SN1 Explain the order in which 1o (primary) alkyl halides reacted (fastest to slowest) and…

A: The rate of the SN1 reactions depends upon the concentration of alkyl halide only. This kind of…

Q: A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH3 CH3 CH3…

A:

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.