the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be use reagent1 reagent2 reagent3 Product Reactant Step 1 product Step 2 product (acetylene) Answer Bank H3C. H. Na. NH, (1) NaNH, (2) CH, Br H,, PUC (1) NaNH, (2) CH, CH, Br HC=C-CH,CH, H. CH3 CH H,C-C=C-CH, CH, HC=C-CH, HC=CH HBr H. CH3

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Construct a three-step synthesis of trans-2-pentene or trans-pent-2-ene from acetylene by dragging the appropriate formulas into
the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used.
reagent1
Step 1 product
reagent2
Step 2 product
reagent3
Product
Reactant
(acetylene)
Answer Bank
H3C.
Na, NH,
(1) NANH, (2) CH, Br
H,, Pt/C
(1) NaNH, (2) CH, CH, Br
HC=C-CH,CH,
3
H.
CH3
H.
CH3
HBr
H,C-C=C–CH, CH,
HC=C–CH,
HC=CH
H.
CH3
Transcribed Image Text:Construct a three-step synthesis of trans-2-pentene or trans-pent-2-ene from acetylene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. reagent1 Step 1 product reagent2 Step 2 product reagent3 Product Reactant (acetylene) Answer Bank H3C. Na, NH, (1) NANH, (2) CH, Br H,, Pt/C (1) NaNH, (2) CH, CH, Br HC=C-CH,CH, 3 H. CH3 H. CH3 HBr H,C-C=C–CH, CH, HC=C–CH, HC=CH H. CH3
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