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Please use a drawn example to demonstrate the purpose and steps of a 3 position synthesis...
3. (20 points) A linkage is to be designed to carry the object in Figure 1 from position R to position P at the orientations shown. The chosen values are given as z 2.40, ø - 100° for Z at position 1 and B3 1209. Use analytical synthesis without regard for the fixed pivots shown to obtain W for the left dyad of the resulted four-bar linkage. (30 points) A linkage is to be designed to carry the object in...
Please answer the following: 1. Outline the steps involved in the Gabriel synthesis of 3-amino-2-methylpentane. 2. Draw the structure of the product likely to be obtained from the reaction between acetoacetic ester, bromobenzene and 2 molar equilalents of sodium amide (in liquid ammonia). Give a mechanism for its formation in detail.
Please answer the question below: use this as an example follow the same steps please! thanks 3. (10 points) Find the modular multiplicative inverse of 14 mod 33 using the Extended Eu- clidean Algorithm. Example 3. Find the multiplicative inverse of 8 mod 11, using the Euclidean Algorithm Solution. We'l organize our work carefully. We'll do the Euclidean Algorithm in the left column. It will verify that god(8,11) = 1. Then we'll solve for the renainders in the right column,...
can you please solve everything 9 Give an example of a synthesis that requires the protection of an alcohol. You may use any reaction, any organic compounds. You must show the reaction that does the protecting. Acetylide ion reacts with cyclohexanone, followed by acid workup. Write a complete mechanism. 10. Identify the compound that gives this NMR spectrum. The compound has carbons. 11. 4
Please show the steps. Thanks! the reactions below: 14 nearh 1 ntet 7. Show a synthesis of 2,6-dipehnylhexan-1-ol from ethyne and styrene (vinylbenzene): (8 pts) Styrene = 8. Suggest a synthesis for 2,3-octanediol using 1-bromobutane as your only source of carbon atoms. You may use another other reagents as necessary. (8 points)
typo: chemdoodle just means computer drawn chemdoodle = computer drawn The following pre-lab tasks must be performed individually, typed and printed out and brought to the lab for the first experimental session. Do not use your lab notebooks for this purpose. 1. Using ChemDoodle software draw a reaction mechanism (appropriate arrows, transition states, lone pairs) of imine formation upon reaction of aniline with benzaldehyde. 2. Imines are important synthetic intermediates. Provide synthetic scheme -not mechanism (ChemDoodle drawn) showing synthetic transformation...
Ignore red/pencil markings. Please write all steps legibly thank you. . (30 points) The bucket of the front end loader shown is controlled by a linkage GHDB and arm AFJ.The linkage is comprised of link GH, Dar HDB, and cylinder BC. The arm AFJ which is connected to the bucket at J and the linkage at D is controlled by hydraulic вс. cylinder EF. For the position and loading shown, determine the force exerted by cylinder 20 in. 28 in....
Purpose of the following guestion: Demonstrate knowledge of basic economic definitions and ability to use data to find optimal solution. (10 points) Your total benefits from consuming different quantities of gasoline each week are shown in Table 1. Table 1: Benefits of Consuming Gasoline Gallons per Week Total Benefit Marginal Benefit 15 21 26 30 2 36 a. Complete the marginal benefit column starting with the step from 0 gallons to 1 gallon per week. b. The price of gasoline...
Propose a stepwise mechanism for the synthesis of N,N-diethyl-m-toluamide (DEET). please show all steps! thanks (CH,CHy), WH -CH,CH) NHCr N(CH, CH,) SOCI -HCI CAM3 -5 CAM
Please go through each step of this synthesis problem and show each reactant bwtween steps! It is very important that they are correct so please make sure your answer is right! thank you so much! E. SYNTHESIS: (12 points) cohols, alkenes synthesize the molecule below using any of the following reagents: a and/or alkynes of three carbons or less, any inorganic reageAts, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. HO OH HO