Q: 12. Show how to convert cyclopentene into these compounds: ams bos Br (b) (a) Br (c) (d) OH Br
A: We have to predict the reagents for given conversions.
Q: Markovnikov Hydrohalogenation – HX (SYN & ANTI) :CI: H-CI: Scenario A H. A B H H-CI: Scenario B :CI:…
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Q: 4. Draw the starting materials of the following cycloaddition products: a) H3C. SO,Ph H3C Br b) c)…
A: When π4 and π2 system undergo cycloaddition reaction under thermal condition then cyclohexene ring…
Q: Draw the products formed when the following diene is treated with Og followed by CH,SCH3.
A: Ozone is a very strong oxidizing agent. It is used for production of ketone or aldehyde from alkene.…
Q: 5. Reactivity to EAS CHO TEN BEN MEN DECREASING REACTIVITY TO EAS:
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Q: Br u
A: If the highest priority functional groups are on the same side, then the stereochemistry is Z,…
Q: What diene and dienophile are needed to prepare the following compound? Choose the single best…
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Q: Acyclic conjugated dienes may exist in two conformations, as shown below. Based on differences in…
A: Trans conformar is conformar in which bulkier group are on opposite side.
Q: A В Least Stable Most Stable D
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Q: Which of the following compounds undergo Friedel–Crafts alkylation with CH3Cl and AlCl3? Draw the…
A: INTRODUCTION: Friedal-crafts alkylation reaction is defined as when benzene is treated with CH3Cl in…
Q: Rank the following dienes in order of decreasing heat of hydrogenation. Me Me Me Me Me A B Me Me Me…
A: Heat of hydrogenation is the measure of stability of alkenes. The most stable alkene will have less…
Q: Draw the mechanism and product for each of the following Diels–Alder reactions.
A: The given reactions are the example of [4+2] cycloaddition reaction. The reactions take place in the…
Q: Which diene below is most stable (draw your choice)? Explain your choice.
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Q: Which diene has conjugated double bonds? b) d) e)
A: Conjugated double bonds are the two or more double bonds that are separated by a single bond.
Q: (1) Which is an isolated diene? (2) Which is an alkene with possible rearrangement product (1,2-H…
A: Following are the appropriate answers of the given questions.
Q: Which of the following is an isolated diene? I. II. III. IV. V.
A: Dienes are the compounds which contains the two double bonds in their structure.
Q: In a Diels-Alder reaction, compound will react the fastest and _ will react the slowest. CN NH2 CN…
A: Dienes react with dienophiles in Diels alder reactions. Dienophile should have electron withdrawing…
Q: Draw all possible stereoisomers of hepta-2,4-diene and label each double bond as E or Z.
A: In the naming of geometric isomers, E, Z notation are used instead of cis, trans teams.Where, Z…
Q: 4. Draw the structures for the products of each of the following Diels-Alder reactions ČO,Me NC. CN…
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Q: Supply the required reagents to carry out the foll owing transformanion in the correct order, wma…
A: When carboxylic acid ( F. Hexanoic acid) treated with Bromine in presence of Phosphorus tribromide…
Q: (c) In the Diels-Alder reactions below, explain the product that could be formed. (i) H (ii) OCH3
A: A question based on alkene that is to be accomplished.
Q: Dorano the arganic focodued Stuctwe बतुकोहे त मकhe उ्न ं ॐ बेश्रव 1Te with mechanism A A. B2 He…
A: -> it is hydroboration -oxidation first of all addition of B2H6 to double bond then in presence…
Q: 4.) For the following dienes A-G, please circle which organic molecules would not function a dienes…
A: For a diene in Diels Alder reaction, it should be in cis form and conjugated. If a diene is in trans…
Q: Which of the following systems are conjugated?
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Q: Draw the products of each reaction and indicate their stereochemistry.
A: The NBS reagent, which is the source of bromine, in the presence of aqueous DMSO, the anti-addition…
Q: What diene and dienophile are needed to prepare each Diels–Alder product?
A: “Hello. Since you have posted a question with multiple sub-parts, we will solve the first three…
Q: 4.) For the following dienes A-G, please circle which organic molecules would not function as dienes…
A: Dienes are electron rich species which along with dienophile are converted to a cyclic product…
Q: Determine the double bond stereochemistry (E or Z) for the following molecules. F. H3C C A CH3 F. H…
A: Rules for writing the E and Z configuration:
Q: Which one of these dienes is least stable? H3C C=c=c H3C H CH3 A В D E
A: Isolated dienes: Isolated dienes typically show no "special" stability. Their two π-bonds interact…
Q: Which product is the result of a 1,4 addition to the following diene? H-CI C. B D A D
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Q: Which of the following carbocations is the least stable? D. X С. Е. A. N А. В. H. Oc OA E B
A: We know the stability order of carbocation: 3°>2°>1°>CH3
Q: i. Hexa-2,4-diene-1,6-diamine j. 1,4-diaza-cyclohexa-1,3,5- triene
A: To draw structures of compounds from IUPAC name, • Write the principal chain by locating the root…
Q: 9. Which one of the below molecules is the most reactive diene? A O A. A ОВ. В OC.C O D. All of them
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Q: 5. What is a dienophile? O A. "diene-loving" O B. has one pi bond OC. reacts with diene O D. All of…
A: Interpretation - To tell about which one is correct about the dienophile in all the given options…
Q: Place the compounds in order of increasing reactivity in a Diels-Alder reaction. (least reactive…
A: Applying concept of Diels Alder reaction.
Q: Which structure is (S)-penta-2,3-diene? O a. b. E%3D c. O d. none of the other answers O e.
A: Penta-2,3-diene is an allene (one carbon contains two double bonds and is sp hybridized).
Q: a,2,3,3-tetramethylbutane + Oz $lame. b) u,5-dimethyl cyclohexene thnOx/Ha50x, ) 3-metyl_l-butene…
A: Depending on the difference in reaction condition the different type of product is formed .
Q: Select the correct diene and dienophile combination which will produce the following structure. A a…
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Q: Determine the double bond stereochemistry (E or Z) for the following molecules. A В а. А: E;B В: Е…
A: Whenever the higher priority group (high atomic mass or atomic number or bulkier group) are present…
Q: What is an appropriate systematic name for the following compound? Br O…
A: The given compound is a seven-membered cyclic ring with two double bonds and two methyl groups. On…
Q: Draw the products of each reaction. Indicate the stereochemistry of Diels–Alder products.
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Q: Select the correct diene and dienophile combination which will produce the following structure. A a…
A: The question is based on the concept of organic reactions. We have to identify the reagent in the…
Q: Vhich of the following dienes is in the s-trans conformation? II IV V a. d. IV p. II е. V c. III…
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Q: What is the major product of the following Diels-Alder reaction? CN NC CN CN CN CN CN CN CN A. C D.…
A: This reaction is an example of pericyclic reaction. Here two molecule reacts to form a single…
Q: 5. What is a dienophile? OA. "diene-loving" O B. has one pi bond OC. reacts with diene O D. All of…
A: Dienophile :- Alkene or alkyne is known as dienophile , because it accepts π- electrons of…
Q: (a)Which of the following has Z stereochemistry? • Which of the following has Z stereochemistry? A В…
A: Z notation is used when the most priority group is placed on the same side of the carbon = carbon…
Q: Which of the following dienes undergoes a Diels-Alder reaction the fastest? 1 3. 4 O 4 O 1 O 2 5 2]
A: Diels alder reaction require electron rich diene and electrophilic
Q: Which diene yield the following product when reacted with the correct dienophile? CHO CHO
A: Diels elder reaction involves the reaction between dienes and dienophiles to form a product in a…
Q: NC 기 CN NC 소 CN NC
A: Intrdouction : We have to make the products .These are pericylic reactions .
Q: Which position will Br2/FeBr3 substitute? осн a O a. f O b. a O c. g O d. e O e. b O f. d g. C
A: Given
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- Alkynes undergo many of the same reactions that alkenes do. What organic product(s) would you expect when the following compound is treated with 2 equiv H2, Pd/C?Which of the following is the product of the reaction shown in Image 17? a. (C6H5)3COH b.C6H5CH2OH c.(C6H5)3CH d.(C6H5)2CHOHThe SN2 reaction is an example of a nucleophilic substitution reaction. Draw the structure of the two reactants and the mechanism of the reaction. The reaction is 1-bromo-3-ethylpentane reacts with cyclohexanol under basic conditions.
- From what alkyne might each of the following substances have been made? (Green = Cl.)Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H2O, H2SO4; or [2] BH3 followed by H2O2, −OH.Answer all questions Q1. What are the various ways by which alkenes maybe synthesized. Q2. Give two examples each of unsymmetrical alkenes and reagents. Q3. Give three examples of reactions of alkenes which tesult in anti markovnikov addition
- Are terminal alkynes considered weak or strong acids?1. When you add H-Br in a terninal alkene, the product has the rule od Markovnikov? 2. The type pf intermetary thag forms when we add HgSO4/H2SO4/H2O in an alkyl is? Please solve my both questions.thank you.Which of the following reactions results in Markovnikov addition of H2O to an alkene?
- Indane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring.(a) Draw the possible monochlorinated products from this reactionName the following alkene and draw the product of the reaction with KMnO4.the action of halogenated derivatives of alkanes with KOH: CnH2n + 1 Cl + KOH = CnH2n + 2O + KCl is: a) radical substitution b) nucleophilic substitution c) electrophilic substitution d) addition reaction