1 1. Sia2BH Na 2. H,О* 2. H-Ор, NaOH mCPBA Li, Na correct stereochemistry correct stereochemistry

Q: Draw the products of attached reaction. Indicate the stereochemistry of Diels–Alder products.

A: The products of attached reaction can be drawn as The stereochemistry of Diels–Alder products can be…

Q: (c) OH (d) Br ? ? Eight or fewer carbons Acyclic compounds OH Br

A:

Q: 1. Write the IUPAC name for: Stereochemistry CH3 CH3 CH3 CI CI -H- CI NH2 -NH2 H- -NH2 ČH2CI ČH2CI…

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Q: Draw the structures of organic compounds A and B. Indicate stereochemistry where applicable H2 H20…

A: H – C ≡ C – H → H – C ≡ C                                          ↓ CH2CH2CH3-Br…

Q: Name the following molecules according to the IUPAC nomenclature system. Indicate stereochemistry…

A: IUPAC name of following compounds

Q: b. -CH3 H2, Pt_ CH3

A: The products of the following compounds are:

Q: H Br H- Br Type of reaction? Isit stereospecific? #of streoisomeric products? Relationshie between…

A:

Q: Br u

A: If the highest priority functional groups are on the same side, then the stereochemistry is Z,…

Q: Determine the stereochemistry of the numbered carbon. Write R or S 16. 17. 18. 19. 20.

A: R/S nomenclature is based on the CIP rule which states that higher is the atomic number of directly…

Q: व) होप्हभरीर लाय hanोइनक पजमकि P००वैपटको ०सै the fallowing orea tiog incladting stereochemisty कल…

A: ->Alkyne has nucleophilic character hence it give electrophilic addition reaction to triple bond.…

Q: Draw all the isomers of C,H10: Clearly show stereochemistry if stereoisomers are possible. Step 1:…

A: In linear form stereochemistry can show on double bond if grouping is different on double bond

Q: styrene as shown in the box? H R• + ? нн H R н-с-с- R-C-с. А) B) нн нн H R R-ċ-C нн C) D) нн I-U O-I

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Q: What is the stereochemical configuration of this alkene? O 2E, 4Z O 2Z, 4Z 2E, 4E O O 2Z, 4E by

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Q: conc. H2SO4 180 °C Но

A: The reaction given is,

Q: X= muclaophile 3. C-C-2-e + ビメ → + HX > what in the diterence? 00 ニ- 2HaC 0ー ーとーロH +N-Cビ-0H →…

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Q: Draw the products of each SN2 reaction and indicate the stereochemistry where appropriate. CH3 CuCI…

A: a) The product formed is,

Q: Draw the products of each SN2 reaction and indicate the stereochemistry where appropriate. а. + OCH3…

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Q: 5. 5. ОН `ОН CrO3 H2SO4, H2O 1. NaH 2. Br

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Q: Determine the product of the ff. rxn НО H2SO4 А. C. D. All of the given choices B.

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Q: Show the product(s) with the correct stereochemistry, if applicable. -CH2CH3 1. ВНз, THF 2. Н2О2,…

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Q: stereochemistry when applicable. Br a) b) c) d) c) Br Br 1) Nal 2) NaCN, acetone 1) NaOC(CH3)3, heat…

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Q: ! wite Out He stepwie mechanism, including intermediaves or 1. transition state for : Na oH > Br.

A: The given compound is reacted with base to give alkene compound.

Q: From HzSO4 conc. 2) MCPBA + EN 3) Hz + EN

A: Using concept of reaction mechanism, stereochemistry of molecules and selectivity of reagents.

Q: a) b) Draw the product of the first step as well as the second step including stereoisomers مهم O₂N…

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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: iupac nme include stereochemistry if ncessary

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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: OTs KCN (CH3),C. H.

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Q: Draw all the isomers of C,H10- Clearly show stereochemistry if stereoisomers are possible. Step 1:…

A: constitutional isomer have same molecular formula but different arrangements.

Q: Draw the products of each SN2 reaction and indicate the stereochemistry where appropriate.

A: (a) (S)-1-chloro-1-duetiro ethane undergoes SN2 with methoxide ion to form (R)- 1-duetiro-1 methoxy…

Q: Find the single mawor orgeenic producs indicated transtormation. Use He reagent in a reasonable way.…

A: Sulfonation is a reversible reaction that produces benzene sulfonic acid by adding sulfur trioxide…

Q: Name  the compound, showing stereochemistry if relevant

A: There are three carbon atoms in the long chain. Number the chain and see that the substituents and…

Q: 1. H2. Lindlar's catalyst 2. HCI Use the wedge/hash bond tools to indicate stereochemistry where it…

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Q: 17. How many stereoisomers exist for the strueture below? a. two optically active and one meso b.…

A: We have to tell number of possible stereoisomers for the given molecule.

Q: a) Draw the structures and specify the stereochemistry of compounds A-C. Pyridine NaNg i) LIAIH, в…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: What is the absolute stereochemistry of C2 and C4?

A: The asymmetric carbon is categorized as chiral center. Its configuration is determined by using…

Q: Draw the products formed in attached reaction and indicate stereochemistry.

A: Acetylide ion displaces oxygen to form the product. In this reaction, the epoxide ring opens. This…

Q: How many stereoisomers of 3-bromo-butan-2-ol exist? 01 02 O5 4.

A: The structure of 3-Bromo-butan-2-ol is:

Q: CH3 CH;CH,-C-0-CH3 ČH3 HI (2 еquiv)

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Q: Br, CH,0 CH3 (A) - hv → (B) major product B is :- (1) -Br (2) ОСН, (3) (4)

A: A synthesis is the manufacture of chemical compounds by the reaction from simpler materials or…

Q: Which compounds are meso compounds?

A: A meso compound has two or more chiral carbons but it is optically inactive due to the presence if…

Q: (a) Draw all stereoisomers formed by monobromination of the cis and trans isomers of…

A: A question based on alkanes that is to be accomplished.

Q: Draw tructu f he ajor rganic roduct f he ollowing reaction. CH2 1. Hg(OAc)2, H20 2. NaBH4 CH3 • In…

A: Hg(OAc)2 along with water and followed by NaBH4 are used to oxidize an alkene to alcohol.

Q: Draw the products of each reaction. Indicate the stereochemistry of Diels–Alder products.

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Q: To the right of each name provide a correct structure. Show stereochemistry clearly in each case…

A: A question based on nomenclature that is to be accomplished.

Q: 1. HgSO4 H20 Cl2 2. NABH4 how stereochemistry

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

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 carbocation is more stable? CH3C+H2 or H2C=C+H

A: The more stable carbocation is to be identified: CH3C+H2 or H2C=C+H.

Q: Describe the stereochemistry. CHO F CH2OH H;C- CN ČH,CH3 O 2R, 3R 2S, 35 2S, 3R O 2R, 3S

A: During R and S nomenclature ,we use CIP rule .The highest atomic number group is marked 1st then so…

Q: Me Me OMe OMe OH & OH OMe COMe BF 3'OEt2 Mgl2 A B show relative stereochemistry show relative…

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Organic Chemistry of Metabolic Pathways

Metabolic pathways allude to the arrangement of chemical catalyzed reactions that lead to the transformation of a substance into the final product. Metabolic pathways incorporate a progression of reaction where the substrate is changed continuously and the transitional metabolites are persistently recovered.

Glucogenesis

Glucogenesis is a metabolic pathway in which glucose is produced from carbon substrates that are not carbohydrates. This process is observed in plants, animals, fungi, bacteria and other micro organisms. The general  definition for glucogenesis or gluconeogenesis is as follows,