

2. Perform resource allocation for the following project. Resource limits are 5 labors and 4 help...
2. For the following project draw a node network and a bar chart. Then perform resource leveling trying to reduce the daily resources needed to no more than 8 laborers per day. If you cannot get it down to 8, manually shift resources so that the project starts low and gradually increases towards the middle and gradually decreases toward the end of the project Duration (days) laborers Activity IPA А 6 2 В 2 C 8 3 5 А, В...
Deduce the correct structures that correspond to the following 1 H NMR data. C 4 H 9 Cl δ 1.3 (doublet, 6H) δ 1.6 (nine peaks, 1H) δ 3.4 (doublet, 2H) C 5 H 10 O 2 δ 1.2 (doublet, 3H) δ 2.1 (sextet, 1H) δ 2.2 (singlet, 3H) δ 2.5 (br singlet, 1H) δ 3.8 (doublet, 2H)
Draw the structure that would be responsible or the following
spectra:
5. CH.0;septet (1H), singlet (3H), doublet (6H) 11 10 8 7 6 4 3 2 1 0 5 ppm 6. C1H1402, multiplet (5H), singlet (2H), triplet (2H), multiplet (2H), triplet (3H) E 11 10 9 2 ppm
Question #2. (20 marks) The following table shows activities related to a small project and their weekly usage of labors. Smooth (level) the resource usage so that a preferred resource usage is obtained. Activity IPA Duration week) Labor/week start start start Selo F G H Question #3. (15marks) For the project information of question2 above, and referring to the field report below, perform a revised schedule, then comment on it. At the end of week 5 the following field information...
I need help with the assignment there are 4 1. 3.9ppm, singlet, 3H 2. 7.4ppm, triplet, 2H 3. 7.6ppm, triplet, 1H 4. 8.1ppm, doublet, 2H
5. (10 pts) Compound A, C10H1002, shows the following IR and NMR spectra. Propose an acceptable structure. 3000 1690 ose 3H, s 3H 2H 1H, 1H 14 12 10 8 6 2 0
Predict the proton NMR of compound 5, 5-(2-(diethylammonio)-5-oxocyclopent-3-en-1-yl)-2,2-dimethyl-4-oxo-4H-1,3-dioxin-6-olate, by labeling each inequivalent hydrogen with a letter and creating a table with each inequivalent hydrogen in a separate row in the below table. Proton Label Chemical Shift (ppm) Integral (e.g., 1H,2H, 3H…6H) Coupling (e.g., singlet, doublet, triplet) PLEASE fill out table when answering. Proton Label Chemical Shift (ppm) Integral (e.g., 1H, 2H, 3H...6H) Coupling (e.g., singlet, doublet, triplet)
operating systems
Question 2: (4 Points) Consider the following Resource allocation Graph: R P R P P R P R Find its equivalent wait-for-Graph and show the cycle that exists in the resulting graph.
1. NBS 2. Mg, ether 3. 4. H2Cr04 5. SOCI2 6. CH CH OH Work out the synthesis on a separate sheet of paper, and then draw the structure of the final organic product. The 'H- and 'SC-NMR spectra for an unknown compound with molecular formula C H1402 are shown below. Deduce a structural formula for this compound. 1H-NMR 13 C-NMR 0.92 (d, 6H) 1.52 (m, 2H) 1.70 (m, 1H) 2.09 (s, 3H) 4.10 (t, 2H) 171.15 63.12 37.31 25.05...
lect the major product of the following reaction. 1) 2 CH3MgBr 2) H2O 34) Ozonolysis of 1 mole of 4-octyne yields 2 mo this reaction- the 'H NMR spectrum spectrum for es of a single product. Select the product of IR spectrum spectrum for the product is shown below. 1) 03 2) H20 1H, singlet |3H, triplet OH 2H multiplet 2H, triplet c) ~ OH d) n 0 10 16 14 12 ppm