The Answer for the above question is option B.
Option B. 4,1,3,2
In the following order :
4) Direct search markets.
1) Brokered markets.
3) Dealer markets.
2) continuous auction markets.
61) Rank the following types of markets from le integrated and organized: 61) ast integrated and...
4. Rank the following compounds from least to most basic. V. iv. lii il. NH2 A. i< iv < iii< v< i B. ii< v< iv < ii < i C. i< ii< ii < iv <v D. i< iv<v<ii < ii
4. Rank the following compounds from least to most basic. V. iv. lii il. NH2 A. i
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9. Rank the following from most to least acidic CI COOH COOH coOH COOH IV A. I II III >IV B. II I IV> III C. III IV II > I D. IV III I > II E. III IV I II 10. Which hydrogen is the most acidic in the molecule shown below? C A 11. Why are ketones less reactive than aldehydes? A. Ketones are less sterically hindered. B. Carbonyl carbon of ketones...
(Clicker) Rank the following from weakest to strongest IMFs I. CH2 = 0 II. CH4 III. H2O2 IV. KCl(aq) A. I II B. II I C. IV III I II III 1. CH2 = 0 II. CHA III. H2O2 IV. KCl(aq) A. I II B. II I III C. IV III 1 D. III i IV E.Impossible to determine
3) Identify the first mechanistic step in the reaction shown below. H2O OH Lilia ci H-Ö: H-02 4) Rank the following from least reactive to most reactive towards nucleophilic acyl substitution. NH2 ОСН3 III IV a) II <I< IV < III b)I<IV < II < III c) III <IV <I<II d) I< II <IV < III
Rank the following fund categories from most risky to least risky: I. Equity growth fund II. Balanced fund JII. Sector fund IV. Money market fund Multiple Choice IV, I, III, I IlII, II, IV,I I, II, III, IV III, I, II, IV
Canvas → XCO Question 13 2 pts 56. Rank the following carboxylic acid derivatives in decreasing order (most to least of teachiy towards cheople wh o "NH2 A) I > IV > III > 1 B) II > III > IV> C) I>III > I > IV D) III > IV > II > E) IV > I > III > 11
What is the IUPAC name of the following compound? 4 Rank the following alkenes from most to least stable. ОН OH ОН IX M A. I > || > III B. I > III > 11 C. II > III > 1 D. III > II > Which carbon would form the most stable carbocation? A D В С Which of the following is a wax at room temperature? A. B. C. D. E. None of these
SE ATO 1800A . Rank the following resonance structures from MOST to LEAST stable a. III > I > II b. II > I > III c. II > III >I d. I > II > III I > III > II
Which of the following alkyl halides will undergo the low it so reaction? Rank the following compounds from most to least reactive in an S_n1 reaction. l>IV>ll>lll ll>l>IV>lll lll>IV>l>ll IV>l>ll>m IV>IH>I>U Rank the following compounds from most to least reactive in an S_N1 reaction. >IV>II>III B) ll>lll>l>IV C) lll>ll>l>IV D) l>UI>ll>IV E) IV>II1>I>>> Predict the product for the following S*_n1 reaction.
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Rank the acidity of the protons shown in the picture (from most acidic to least) I > II > III = IV IV > I = II > III IV > I > II > II I > II > IV > III What accounts for the difference between the acidity of proton (IV) and protons (I and II)? (may be more than one answer) Feature 1: energy and entropy stabilization Feature 2: energy and entropy stabilization...