Q-3- complete Four of these equations 1- Benzene + HNO - H;SO4 2- Iso-butane + CL, --- 250 - 400C and 3- Propyne + Br2 + Brz 4- 2,3- dibromo butane + Zn --- - 5- Propychloride + Mg in dry ether -------- + HOH----- ..........
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- What functional group is at 763ppm? For HNMR at about 2.3ppm is it a quintuplet? How do I get the structure from this?Show the wurtz reaction of 1-fluoro-2-methylpropane and name the productsWhen 2-methylpropane is monochlorinated in the presence of light at room temperature, 36% of the product is 2-chloro-2-methylpropane and 64% is 1-chloro-2-methylpropane. From these data, calculate how much easier it is to remove a hydrogen atom from a tertiary carbon than from a primary carbon under these conditions.
- Hi there, can someone please help me solve this problem? Please make sure to clarify all steps taken to go about solving for the products and explain various terms and rules that should be known or correlate with the question. I'm using these questions to study for our final exam and need some extra clarification on rules and steps. Thank you very much in advance!Last question for tonight. I am told I have the following nreagents in this order: 1 Br2, hv, CBr4, then 2) H2O, then 3) CrO3, then NaH, THF and finally 5). CH3I, THF. The product is 3-methyl-2-butanone. Can't find the right alkane as my starting material.How to convert how to convert 1-Hexene to Hexanol using math. Please show work step by step on paper
- This is not two separate questions; it’s just one question. I just moved the model around so you could see the full structure. Thanks! :)Please draw the line structures for the C8H17+ carbocations that have the carbon skeleton below And please circle the most stable carbocation4 what is the ftir interpretation of 1-chloro-1-methylcyclohexane?
- The functional groups in an organic compound can frequently be deduced from its infrared absorption spectrum. A hydrocarbon exhibits no bands above 3000 but gives weak absorption at 2200 cm-1.Relative absorption intensity: (s)=strong, (m)=medium, (w)=weak. What functional class(es) does the compound belong to? List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly.Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like 10 to 20 cm-1. The functional class(es) of this compound is(are)fill in the blank 1.(Enter letters from the table below, in any order, with no spaces or commas.) a. alkane (List only if no other functional class applies.) b. alkene h. amine c. terminal alkyne i. aldehyde or ketone d. internal alkyne j. carboxylic acid e. arene k. ester f. alcohol l. nitrile g. etherFrom the data in Figure 4-12 and Table 4-1, estimate the percentages of molecules that have their substituents in an axial orientation for the following compounds: (a) Isopropylcyclohexane (b) Fluorocyclohexane (c) Cyclohexanecarbonitrile, C6H11CNI need to know the names of these two structurers for my notes but I am not sure how to name them.