Q: Why are boiling pointsof ethers often slightly higher than boiling points of comparable alkenes?
A: The general formula of ether is R-O-R' and the general formula of alkene is (-C=C-). The general…
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Q: Draw the structure corresponding to each IUPAC name: (a) 5,5-dimethyl-3-heptyne; (b)…
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Q: Draw the structures of two specific ethers that have the formula C4H10O
A: Structures of two specific ethers that have the formula C4H10O
Q: Give the IUPAC name for each molecule depicted in the ball-and-stick models.
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Q: Give the IUPAC name for the following ether
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Q: Write the IUPAC name for compound
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Q: Draw a cyclic ether with molecular formula C5H10O
A: Given Molecular formula = C5H10O Structure of Cyclic ether = ?
Q: Write the IUPAC name for compound.
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Q: Draw structures for the four constitutional isomers of molecular formula C4H10O that contain an OH…
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Q: Write down the IUPAC name of the structure shown.
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Q: CN
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Q: Give the IUPAC name of the following compounds D, E AND F ONLY
A: A question based on nomenclature that is to be accomplished.
Q: What is the IUPAC name for this structure and why?
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Q: Write IUPAC and common names for ethers.
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Q: an amount of alkene requires 5.6 liters of HCl under normal conditions to fully act. The same…
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Q: Dehydration of ethyl alcohol yields: A. Ethylene B. Ethanal C. Ethanoic acid D. Ethane
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Q: Write the IUPAC name of each alkene
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Q: CI CH CHy
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Q: Alkenes are not soluble in water because they are
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Q: Write IUPAC and common names for ethers.
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Q: Give the IUPAC name of all three subparts in clear handwritten paper!
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Q: What alkane is formed when each alkene is treated with H2 and a Pd catalyst?
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- Please advise if these models resemble the cis-2-bromocyclohexanol & trans-2-bromocyclohexanol. Can you please advise on the priority numbers of each substituent. I am confused from the reading. Is the proproty a single element, the group of elements, the left and right carbon atoms? Please advise and give commentary on Br. & Methyl group oriantation related to the doubl carbon bond plain. And if you can provide a visual that would be even better for the futre, the more detail the better my study notes will be. Thank you. Justinplease provide the machanisms of 1a, 1e, 1fCompound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-yne
- What is the strongest IMF in pure 2-octanone? I know it is a ketone and has some polarity due to this, but the carbon chain so long, I wonder if london dispersion forces are stronger?1. Using Br2 in C2H4Br2 will result in HBr and ______. a. C2H3Cl3 b. C2H4Cl3 c. C2H2Cl3 d. none of the above 2. How many halogenation are posible in propane? a. 3 b. 8 c. 6 d. 10 3.Sulfonation of pentane will result in ________ and water. a. C5H11SO3H b. C5H12SO3H c. C5H14SO3H d. none of the above 4.Nitration of hexane will result in ________ and water. a. C6H13SO3H b. C6H15NO2 c. C6H13NO2 d. C6H14NO2 5.How many moles of O2 in heating a C12H26 (dodecane) a. 27 b. 37 c. 24 d. none of the above1. In the reactions involving the three isomeric alcohols with the formula C4H9OH, describewhat each of the following tests showed about reactivity of the -OH group and reactions of 1°,2°, and 3° alcohols.• the test with neutral KMnO4• the test with concentrated HCl2. Predict how the fourth alcohol with the formula C4H10O would react if tested with:• 0.01 M KMnO4• concentrated HCl at room temperatureExtend FurtherUse your observations of the solutions formed in the previous experiments and yourunderstanding of alcohols to complete a table like the one shown below. Research the meltingand boiling points to verify your answers.
- I need help to perdect the ir spectreum digram for the staring matrial and also for it need to draw the staring matrial and labled the functional groups on it and on the ir spec digram I linked an example I made on how it suppose to look, its not the answer just the formatAnswer the following Compounds CORRECTLY by giving the IUPAC NAME OF IT. •Label with proper notations (like hyphen, commas, periods, and grouping symbols) thank u❤️I need help to draw a 4-Nitrobenzyl Alcohol ir spec digram and also for it need to draw the4-Nitrobenzyl Alcoholnand labled the functional groups and on the ir spec digram I linked an example I made on how it suppose to look, its not the answer just the format
- The IR spectrum of a sample contains absorptions at 3050, 2950, and 1620 cm-1. Towhat class of organic compound does this sample most likely belong? ExplainA) alkaneB) alkeneC) alkyneD) esterE) alcoholRank the following groups in order of decreasing priority. −F, −NH2, −CH3, −OHUnknown Results - Solubility Test: - Slightly soluble Ceric Ammounium Nitrate Test: - Positive Iron (III) Chloride Test: - Negative Chromic Acid Test: - Positive Iodoform Test: - Negative Luca's Test: - Negative The known alcohols tested in this experiment are: Ethanol 1-Propanol 2-Propanol 1-Butanol 2-Pentanol 2-Methyl-2-propanol 1-Octanol Phenol Although you didn't carry out every test on all eight alcohols, you should be able to predict the results for the tests on the alcohols that you did not test. If your unknown alcohol is one of these eight known alcohols, which do you think yours is? Can you definitely identify it? Explain your answer using your test results and predicted results.
