Q: H HO, AICI3 H HO HO. HO HO A B D
A: It is friedel craft alkylation reaction. -OH group is ortho para directing group -CHO is meta…
Q: Ph. OTs OTs NaOH NANH, ? ? NaOH ? A В C Ph. CI NaOH dilute NaOH ? D
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Q: The best reagents to carry out the reaction at right would be: a. O c. CH₂ Hg(OAc), H₂O NaBH4 KOII…
A: The given reaction is : What is the best reagent to carry out this reaction towards right side ?…
Q: 10. Draw a reasonable mechanism for the following reaction (cat. = catalytic %3D amount). OH H2SO4…
A: Rearrangement of carbocations.
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: In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1,…
A: As per rule only three subparts can be answered.
Q: 1. Show a detailed mechanism for the following reaction. 1. Cl2, NaOH HO, 2. H3O*
A: Haloform reaction :- Formation of carboxylic acid from Ketone in presence of Halide ( Chlorine ,…
Q: 5. Provide the mechanism for the Wittig reaction below. H3C H3C- FPPH3 CH3
A: The Wittig reaction is the chemical reaction of aldehyde or ketone with a triphenyl phosphonium…
Q: H+ SOCI2 NH3 CH3 ?
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Q: (b) OAc HOAC MsO
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Q: B. Supply the missing arrows to complete the reaction mechanisms below. For each of the reactions,…
A: Here we are required to draw the curly arrow to complete the reaction
Q: 1) NaOCH3 H3CO OCH3 2) H+
A: Dieckmann condensation is the intramolecular chemical reaction between diesters that gives beta keto…
Q: 3) Write a detailed mechanism of: CH, CH. HNO" H'SO O,N
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Q: Show a reasonable mechanism for how the following reaction comes about OH NaONO H30* H2N
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Q: Br NaOCH3
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Q: + Zn - 35 °C Ме-Li + Br + Mg
A: These are the general reaction: In 2nd reaction H is an acidic proton it lose H and gain…
Q: لمد HO HO.
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Q: Select the major product of the reaction sequence below. OH NHČCH, NHCHCH, NHCH,CH, NHCHCH, NHCH,CH,…
A: Step 1: Fridel Craft's Acylation at the para position.Step 2: Reduction of amide and ketone group to…
Q: HO Provide a mechanism for the transformation below. HO H,O/ CH;OH :0:
A: A reaction mechanism is the order of basic steps by which a chemical reaction occurs. A reaction…
Q: II Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…
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Q: 10. Draw a reasonable mechanism for the following reaction (cat. = catalytic %3D amount).
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Q: Practre ono 3 Write a detailed mechanism for this transformation H HCI ОН H20
A: This reaction consists of two step which is explain below
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: 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: 3) write a detailed mechanism of: OH он CHIČCI AICL3
A: The above reaction is an example of friedal-craft acylation reaction . It is a type of electrophilic…
Q: 2.) Show the complete mechanism and the major product formed from the reactions below. OMe CH,CH,OH
A: The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group…
Q: 2) Write a detailed mechanism for the following reaction: H2S04 CH;CH;C=CH + H,O CH;CH¿CCH3
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Q: 2) Propose a mechanism for the following reaction (show all arrow pushing). Note that DgO* has…
A: Two molecules which have same molecular formula but different connectivity and they are easily…
Q: Br NH2 NANH2 NaBr
A: The reaction of bromobenzene with sodium amide results in the generation of aniline and sodium…
Q: Propose a detailed mechanism for the reaction below. لعلام , AICI3
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Q: 3. Draw the mechanism for each reaction below; HO H, H CH,CH CH,CH,NH, HyC H. H (pH = 5) H. 1. Ph,P…
A: Note: As per company policy we are supposed to attempt first three subparts only. Please repost…
Q: Propose a plausible mechanism using curved arrows that shows the 10. formation of product A only.…
A: The organic reactions are carried out in more than one step. It is carried out with the help of…
Q: 2) Write a detailed mechanism for the following reaction: H2SO4 CH;CH,C=CH + H2O CH;CH,CCH3
A: Hydration reaction of Alkyne takes place in acidic medium as follows:
Q: 4. Propose a mechanism for the reaction below. ( HS SH cat. H
A: Reaction- In analogy for the formation of acetals from alcohols and acid, treatment of…
Q: 4. For the following, a) predict the product and b) using curved arrows to show electron movement,…
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Q: Provide a plausible arrow pushing mechanism for the reaction below. OH OMe TSOH, H20 OMe
A: The answer is mechanism
Q: rite the mechanism for the reaction below. -OH + CH3OH
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Q: Which compound is a major product of the reaction sequence shown in the box? 1. EtO Na+ OEt 2. HСI,…
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Q: For the substitution (SN2) reaction below circle the nucleophile and draw a box around the…
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Q: Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible…
A: The complete reaction is given below.
Q: Ph Na Oet Eto OEt
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Q: 9. Draw a complete, detailed mechanism for the reaction below, and product(s). CH,OH NaOCH3
A: Ester are derived from substitution reaction of carboxylic acid and an alcohol, they are volatile…
Q: 1. Give a mechanism of following conversion CH,OH
A:
Q: 5) Show the complete mechanism for an E2 reaction with 1-bromo-2-tert-butylcyclohexane
A: Answer - 1-bromo-2-tert-butylcyclohexane - A chemical structure of a molecule includes the…
Q: Identify the elimination product(s) formed in the reaction below. Br H,0 CH3 CH(CH,), O a. CH(CH,)2…
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Q: HCI CH3-CH2-CEN CH3-CH2-C-OH + NH,CI H2O
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Q: Propose a mechanism for the reaction shown below. ÇI OH ONH2 + CI Нeat NO2 NO2
A: NOTE: The product given is incorrect and the correct product will have NH2 group in the place of OH.…
Q: CH3 o-nitrotoluene CH3 NH, CI NO2 CH3 o-toluidine NH3*,CI CH3 CI 2-chloro-N-o-tolilpropanami NH,HCO,…
A: The solution is given below:
Q: 3) Write a detailed mechanism of: CH. CH HNOT HYSO! "NO.
A: Given is the reaction between Toluene in presence of nitric acid and sulfuric acid.
Q: 1. Excess LIAIH4 MeO НО 2. H2о
A: Given reaction: We have to write the mechanism of the reaction.
Step by step
Solved in 3 steps with 2 images
- Indicate the complete mechanisms for each step of the synthesis below.Why we need step 3 before step 4? a. Because the nitro group increases the electrophilicity at the ortho positions which is where the bromine is added. b. Because the amine group is a strong ortho, para director which is what controls the regiochemical outcome of this bromination. c. Step 4 is unessesary. The symmetry of compound 3 allows for the bromination to be regioselective and give compound 5. 5. There will be a mixture of products because there is no selectivity for a major product.Show the reaction mechanism for the formation of:a. RCONH2 from the reaction of RCOOR’ with NH3
- Please give me the final product following reaction . Feel free to write out each step! thatd be greatly appreciated!What is the mechanism of the above reaction (i.e. SN1, SN2, E1 or E2)? Explain your choice in one sentence based on your answer in (i) above.In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1, SN2, or E1, or even 2 of them). Then draw the product(s).