3. What is the IUPAC name of the following compound? Give correct detailed Solution A. (S)-3-ethynylbicyclo[4.2.0]octan-1-ol C. (S)-7-ethynylbicyclo[4.2.0]octan-1-ol E. (S)-3-ethynylbicyclo[4.2.2]octan-1-ol G. (R)-1-vinylbicyclo[4.2.0]octan-3-ol HO CECH H B. (R)-3-ethynylbicyclo[4.2.0]octan-1-ol D. (R)-7-ethynylbicyclo[4.2.0]octan-1-ol F. (R)-3-ethynylbicyclo[4.2.2]octan-1-ol
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- Please see the screenshot below. Answer in clear and detailed step by step solutions, don't use cursive handwriting! Thank you!Draw the structure of the following compounds. Use line-angle structural formula. 1-bromo-4-ethyl-5- methylcyclohexane 3.7-dimethyl-5-propylnonae* 5-chloro-1- ethylspiro[2.5]octane 2-bromo-4- methylbicyclo(3.2.1]octane * 5-cyclobutyl-2-cyclopropyl- 6,8-diethyl-3,7,7- trimethyldecane *4. 3. Complete the equation with a structural formula of the organic product. HH HH C-C H H H С-С' `ОН CC /1/1 HH HH H*/ Cr₂O7²- Write a structure for the oxidation product if ethanol is allowed to react with excess acidic dichromate. CH3CH₂OH excess H*/ Cr2O7²-
- 6.) Predict the product of the following chemical reactions and state where the product (waste) sk waste should be disposed: Example: OH 1. NaBH4, ethanol CH;CH,CH,CH CH;CH,CH,CH 2. H3O* H Butanal 1-Butanol Waste: G704 (Non-halogenated organic solvents) 1. NaBH4, ethanol a.) Cyclohexanecarbaldehyde 2. H3O* b.) Sodium Flouride + 3-iodo-3-methylpentane (hint: substitution or eliminatic 2/3 H3O* c.) Benzoic acid + Phenol РС d.) 3-pentanol H2CrO4 e.) Cyclohexylmethanol(14) Select the correct name for the following compound. H₂ H3C-C H H3C CH (a) 3-methyl-1-pentyne (b) 3-methyl-4-pentyne (c) 3-methyl-1-pentene (d) trans-2-methyl-4-heptene (15) Select the correct name for the following compound. H3C CH H₂ C-CH3 (a) 3-ethyl-2-pentene (b) cis-3-ethyl-2-pentene (c) 3-propenylpentane (d) 3-ethyl-3-pentene C-CH3 H₂ (16) Select the correct name for the following compound. CH3 H3C- -CH3 H3C CH₂ CH OH (a) 4,4-dimethyl-2-pentanol (b) 2,2-dimethyl-4-pentanol (c) 3,3,3-trimethyl-2-butanol (d) 2,2-dimethyl-2-pentanol OHH2CH(CH32, CH(CHJACH3. (CH32CHCH(CH32 SUPPLY THE MISSING REAGENT/PRODUCT(S)/STARTING MATERIAL: O2, spark ? gives only 1. 6 CO2 6 H20 complete combustion one monobromination product H3C 2. CH3 Cl2 light, RT H3C CH3 Cl2 3. light, RT A Ch FeCl 4. For number 2, show calculations for the expected yields of the products. Write the detailed mechanism involved in the production of the major product.
- curri ENO 18) C3 Complete and balance the following reactions a) CH-CH-CH-CH₂ + Bri REAGENTS b) D-Test with potassium permanganate (KMnO4) D.1 Observe the color change. Write (Yes = reaction and NR= no reaction) in the following reactions Condensed structural formulas CI PRODUCTS IF REACTION OCCURS 00:00 Hydrocarbon Cyclohexane (CHz) Cyclohexene (CaH10) Toluene D.2 Draw the condensed structural formula of the reactants and products if any reaction occurred. (CrHe) Reaction with KMnO CICLOHEXANE (C6H12) CICLOHEXENO (C6H10) TOLUENE (CaHo7. The reaction of methoxide anion with bromoethane to yield the ether ethyl methyl ether and the bromide anon (Br-) is an excellent example of a general reaction type called Sy2 (substitution nucleophilic bimolecular): CH,0+ CH,СH-Br a CH3-0-CH,СH; + Br- a. Change in enthalpy is -103 kJ/mol; the change in entropy is + 0.025 kJ/mol-K. Calculate DG at 300K. b. Is the reaction endergonic or exergonic? c. Is the reaction endothermic or exothermic? d. Use curved arrows to show the complete mechanism. Reaction of 2-methyl-1-butene with H-Cl could yield TWO alkyl chloride products. Draw and name 8. them.I put in the answer for compound A, (dimethyl‐lambda4‐sulfanylidene)cyclopropane, and the product 9‐oxadispiro[2.0.44.13]nonane, in the boxes, but it says it's incorrect. What am I not getting?Thank you for your help!
- Estimate the heat released when ethene(CH2=CH2) reacts with HBr to giveCH3CH2Br. Bond enthalpies areC-H : 412 kJ/mol; C-C : 348 kJ/mol;C=C : 612 kJ/mol; C-Br : 276 kJ/mol;Br-Br : 193 kJ/mol; H-Br : 366 kJ/mol. Choose the correct answer:1. 1036 kJ/mol2. 58 kJ/mol3. 424 kJ/mol4. 200 kJ/mol5. 470 kJ/mol7:42 & People Question 33 of 35 Submit Hex-3-ene (C,H,2, molar mass = 121 84.16 g/mol) can be formed from 2 equivalents of but-1-ene (C,H3, molar mass = 56.11 g/mol) using a process called alkene metathesis. Assuming the reaction yield is 100%, how many grams of but-1-ene starting material do you need to add to produce 4.56 g of hex-3-ene product? A) 6.08 g B) 3.04 g C) 1.52 g D) 9.12 gAlkoxides R-O- can be used to synthesize alkenes as exemplified by the reaction shov below, where the symbol (et) indicates that the substance is dissolved in ethanol (CH;CH,OH) used as solvent: Br (1) + HO Br(et) (et) + (et) CH,CH,OH t-but-Br Ethoxide Isobutylene 9. The table to the right shows the results for the initial rate of this reaction when performed under different conditions (four different trials) at 25 °C. What is the rate law for this reaction? a) Rate = k [t-but-Br] b) Rate = k [t-but-Br] [ethoxide] c) Rate = k [t-but-Br]? d) Rate = k [ethoxide]? Trial Initial Initial Initial Rate (M/s) [t-but-Br] [Ethoxide] [isobutylene] 1 0.08 M 0.04 M 6.8 x 10-8 13.6 x 10-8 6.8 x 10-8 13.6 х 10-8 2 0.16 M 0.04 M 3 0.08 M 0.08 M 4 0.16 M 0.08 M