(V) ! show the preparation of the following compounds (v) 2-heptanone starting from acetylene (vi) Cis-3-hexene starting from acetylene D E Focus LE English (US) MacBook Pro
Name the product of the following reaction. cis-3-Hexene. trans-3-Hexene. 1-Hexene. trans-2-Hexene. cis-2-Hexene. Addition of 2 mol of HCl to 1-butyne would yield: CH_3CH_2CH_2CHCl_2 CH_3CH_2CCI_2CH_3 CH_3CH_2CHCICH_2Cl CH_3CH_2CH=CHCI CH_3CHCICHCICH_3 In the presence of excess hydrogen bromide, what is the major product of the addition of HBr to acetylene? 1, 3-dibromoethane 1-bromoethane 1, 1-dibromoethane 1, 2-dibromoethane 2-bromoethane Which of the following compounds is the major product when 1-hexyne is treated with excess HBr? 1, 1-dibromohexane 1, 1-dibromohexene 1, 2-dibromohexene 1, 2-dibromohexane 2, 2-dibromohexane
_________________________________________________________________________________________________________________________________ d. Prepare octane from 1-pentyne, indicate each needed reagents. e. Synthesize cis-2-hexene from 1-pentyne and an alkyl halide. f. Synthesize trans-2-hexene from 1-pentyne and an alkyl halide. Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
Identify the products of cis-3-methyl-3-hexene with hydrogen bromide. Identify the products of cis-3-methyl-3-hexene with hydrogen bromide. (2R, 3S)-3-bromo-3-methylhexane (2R, 3R)-3-bromo-3-methylhexane (2S, 3R)-3-bromo-3-methylhexane (2S, 3S)-3-brom o-3-methyIhexane All of these answers
Sintetize 1) hexene from ethyne 2) Cis-3-hexene from ch2-ch2-Br
a. How can cis-2-hexene be synthesized from butane and the appropriate alkyl halide via an alkyne? b. Provide reagents and a mechanism for the transformation of 3-hexyne into trans-3-hexene. Say which part of the mechanism is responsible for the stereochemical outcome?
Show how to convert acetylene and bromoethane into 1-butene? Show all intermediates
Please need help on QUESTION 4 Show step by step in the synthesis of trans-2-butene from acetylene and an alkyl halide. Convert cis-3-hexene to trans-3-hexene. Calculate % yields of 1 -chloropropane and 2-chloroprpane from monochlorination of propane. Refer to the reaction, cyclohexene + NBS rightarrow 3-bromocyclohene, in Fig. 10-2 (p. 293). Write the propagation in three separate steps.
Given Acetylene make cis-2-pentyne and trans-2-pentyne. Show full mechanism.
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...