1) For the given compounds, denote each different hydrogen and carbon environment and write how many you have of each. A) B) D) (CH3),CHCH,CH,OCH;CH(CH3); CH,OCH;CH,OCH,Br
Q: CH3 CH3CH2. 1. ВНа ÇH3 0 1 NaBH, or LIAIHA 2. H,0 CH3 2. NaOH, H2O2 CH2CH2CHCH2ČCH3 a) b) CH2CI2…
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Q: 1. Write the correct IUPAC names for the following organic compounds: а) Br CH3 H3C (Assign E or Z…
A: IUPAC nomenclature is used to name the organic compound.
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A: The given information shows that the 2,3 dibromoethane reacts with 2 equivalents of a base to give 3…
Q: 1. The structure of compound A is shown below. он NH2 (d) State the possible type of stereoisomerism…
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Q: b. d. Note: Ph -phenyl NHCH,CH3 Ph-N-CH,CH3 CH2CH3 ČH3
A: ◆ The longest continuous carbon chain includes the carbon attached to -NH2 group. ◆ Amines are named…
Q: 1. (cont.) of Cl-S-CF3 CH;NH2 CH3 (i) -ОН CH,CH3 CH3 1. PBr/pyridine () -ОН 2. NaOH/DMSO D
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Q: 1. LIAIH,, ether major product 2 H,0°
A: We have given the organic reaction and we have to find the major product of the reaction.
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Q: H30* ?
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Q: Rank the indicated hydrogen in the following compounds from most acidic to least acidic:
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Q: HC=CH Acetylene + CH,COSH Acetic Acid H₂SO4 HgSO4 H₂C- 0 Vinyl acetate -C=CH₂ Acetylene reacts with…
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Q: write a mechaniSHI 181 CH₂=CH- Los -CH3 + CH3–CH2–CH,—CH 120 OH A -0 d CH₂CH3
A: The given reaction is a example of basic aldol reaction. Aldehyde is more reactive than keton .
Q: Give a clear handwritten answer with explanation needed of each molecule
A: given data predict the solubility in water a) c2h3cl b) CH3CHO
Q: Under certain reaction conditions, 2,3-dibromobutane reacts with two equivalents of base to give…
A: The structure of 2,3-dibromobutane can be written as
Q: 2. Write the correct IUPAC names for the following organic compounds: A. Br (Assign E or Z…
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A: When the given compound reacts with acetyl chloride, an ester is formed.
Q: 1. Write the correct IUPAC names for the following organic compounds: a) Br CH3 H3C (Assign E or Z…
A: The IUPAC name of the given compounds are as follows:
Q: Name each alkene and specify its configuration by the E,Z system
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Q: CH3 H,SO, HO
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Q: butadiene. How would you accomplish this synthesis? ?. H₂C=CHCH=CH₂ H₂NCH₂CH₂CH₂CH₂CH₂CH₂NH2
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Q: Which structure Is aromatic and has six electrons In the conjugated system? Click on a letter A…
A: Aromatic compound which follows huckel's rule i.e. 4n+2 rule where n is natural number.
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Q: Draw the product obtained when cis-2-butene is treated first with Br2 in CH2Cl2, second with NaNH2…
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Q: Complete the following reactions: || C-0-CH,CH, +NAOH- a. b. CH;(CH,),-C-0-CHCH,+H,O CH3
A: Answer of the question given below,
Q: Give the organic product. OH || CH3 H,0 CH,CH3 CH3 CH3 II ОН CH3 CHCH,-CH, CH; CH3 CH3 CH;CH2-CH CH;…
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Q: CH3 CH=CH2
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Q: Tah Here is the chemical structure of 2-methoxypropane: H. H=C–H н :0: Н H-C-C-C-H H. H H. Decide…
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Q: Identify compounds B-G according to the following synthetic scheme. CH₂Br A Mg ether B D D₂O 1.…
A: Products B-G formed as follows,
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- Give a clear handwritten answer Draw the 2 chair confirmations of this structure:a. How many vinylic hydrogens does cyclopentene have? b. How many allylic hydrogens does it have?Resveratrol is an antioxidant found in the skin of red grapes. Its anticancer, anti-inammatory, and various cardiovascular effects are under active investigation. (a) Draw all resonance structures for the radical that results from homolysis of the OH bond shown in red. (b) Explain why homolysis of this OH bond is preferred to homolysis of either OH bond in the other benzene ring.
- what is degree unstaturation of the following ? and draw 2 structures per each numbera. Draw the two chair forms for compound A, being careful to show the stereoisomergiven above. You may use shorthand R in your drawings. Indicate the MAJOR and MINORconformations b. Using curved-arrow convention and the correct chair form of Compound A, show themechanism for the formation of alkene C from Compound A. You may use B: to indicatethe base.Resveratrol is an antioxidant found in the skin of red grapes. Its anticancer, anti-inflammatory, and various cardiovascular effects are under active investigation. (a) Draw all resonance structures for the radical that results from homolysis of the OH bond shown in red. (b) Explain why homolysis of this OH bond is preferred to homolysis of either OH bond in the other benzene ring.
- For the molecule given, prioritize each substituent on the stereogenic carbon, and assign absolute stereochemistry.c options for first box are bromothyml blue, chlorophenol red or thymolphathelin second box is red,blue,orange,yellow,green third box is red,blue,orange,yellow,greenWrite the structure of the compound E,E-2,4-Hexadien-1-ol and label each non-equivalent carbon with a letter, A,B,C..
- Indicate si/re faces of carbons in double bond highlighted in blue, and explain why?Rank the following groups in order of decreasing priority. −CH=CH2, −CH3, −C≡CH, −HA hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.