Click the "draw structure" button to launch the drawing utility. Under certain reaction conditions, 2,3-dibromobutane reacts with two equivalents of base to give three products, each of which contains two new T bonds. Product A has two sp hybridized carbon atoms, product B has one sp hybridized carbon atom, and product C has none. What is the structure of C?
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- Using the information above, predict the relative acidity of the following compounds.Rank the following compounds in order of the expected acidity: In Order of Increasing Acidity (CH3)3NHCl (CH3)2NH2Cl (CH3)2NH3Cl NH4ClFor the 6-carbon molecule below, how would you expect it to break into two pieces? a. two 3-carbon units b. one 2-carbon unit and one 4-carbon unit c. one 1-carbon unit, one 2-carbon unit, and one 3-carbon unit d. one 1-carbon unit and one 5-carbon unit I'm having a hard time identifying the correct location of Beta and Alpha. If the carbonyl beta is the second bond over from carbonyl, then the breakage would occur at bond C3-C4. This would then result in two 3-carbon units, right? The molecule in the image looks like fructose which would result in two 3-carbon units.Which of the following statements about an -NH2 group is FALSE? a. meta director b. activator towards EAS c. increases electron density on the aromatic ring d. stabilizes positively charged intermediates by resonance or inductive effects
- An ion with a positively charged nitrogen atom in a three-membered ring is called an aziridinium ion. The following aziridinium ion reacts with sodiummethoxide to form compounds A and B: If a small amount of aqueous Br2 is added to A, the reddish color of Br2 persists, but the color disappears when Br2 is added to B. When the aziridinium ion reacts with methanol, only A is formed. Identify A and B.All of the following compounds can react as acids. Without using a table of acidities, rank them in order of increasing acidity. Explain your ranking.(a) CH3CH2SO3H (b) CH3CH2OH (c) CH3CH2COOH(d) CH3CHClCOOH (e) ClCH2CH2COOH3) In the mid-1930s, the German theoretical chemist Erich Hückel developed a rule that dealt with the aromaticity of various compounds, which became known as the Hückel Rule. Which (parts) of the compounds listed below are aromatic? Justify your answer based on Hückel's rule. You can treat the rings separately or together as you wish.image iv: colchicine: a highly poisonous alkaloid,obtained from autumn turmeric and used to treat gout.
- 3) In the mid-1930s, the German theoretical chemist Erich Hückel developed a rule that dealt with the aromaticity of various compounds, which became known as the Hückel Rule. Which (parts) of the compounds listed below are aromatic? Justify your answer based on Hückel's rule. You can treat the rings separately or together as you wish. IMAGE IV: colchicine: a highly poisonous alkaloid, obtained from autumn turmeric and used to treat gout.Which of the following statements is FALSE? Select one: a. Aromatics are compound that are conjugated. b. The Cs and Hs in an aromatic compound are equivalent. c. The pi electrons are delocalized around an aromatic ring. d. None of the statements is false.A chemoselective reaction describes a reaction where Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a one enantiomer selectively reacts over another b one diastereomer selectively reacts over another c one functional group selectively reacts over another d one constitutional isomer selectively reacts over another e epoxides are synthesized
- HURRY ASAP I WILL RATE NO NEED FOR EXPLANATION WHICH OPTIN Which one of the following statements about compounds given below is true? Compound 1 Compound 2 CH3CH2SH CH3CH2OH Hydrogen bond strength of compound 1 is less than compound 2 Compound 2 is more easily oxidized than compound 1 Boiling point of compound 1 is more than compound 2 Acid strength of compound 1 is less than compound 2 Compound 1 is more polar than compound 2The shrub ma huang (Section 5.4A) contains two biologically activestereoisomers—ephedrine and pseudoephedrine—with two stereogeniccenters as shown in the given structure. Ephedrine is one component ofa once-popular combination drug used by body builders to increaseenergy and alertness, whereas pseudoephedrine is a nasaldecongestant.a.) Draw the structure of naturally occurring (−)-ephedrine, which has the1R,2S configuration.b.) Draw the structure of naturally occurring (+)-pseudoephedrine, whichhas the 1S,2S configuration.c.) How are ephedrine and pseudoephedrine related?d.) Draw all other stereoisomers of (−)-ephedrine and (+) pseudoephedrine, and give the R,S designation for all stereogeniccenters.e.) How is each compound drawn in part (d) related to (−)-ephedrine?When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?