Nucleophilicity of the groups can be ranked as follow:
-NH2- (Strongest) > -OH- (Intermediate) > H2O (Weakest)
1. Nucleophilicity increases with decreasing electronegativity of donor atom.
-NH2- (Strongest) > -OH- (Intermediate)
2. Negatively charged group is more nucleophilic than their neutral molecule.
-OH- (Intermediate) > H2O (Weakest)
Rank the nucleophiles in the following group in order of increasing nucleophilicity. A. TOH B. NH2...
8. Rank the following anilines in order of increasing basicity, from 1 for weakest base to 5 for strongest base. NH2 NH2 NH2 NH2 NHCHE CN CN Br
Rank the following in order of increasing acid strength (1=weakest acid and 4=strongest acid) 4. (4 pts) Rank the following structures in order of increasing acid strength (1 = weakest acid and 4= strongest acid): HN NH OH OH We were unable to transcribe this image
Arrange the following ions in order of increasing leaving group ability and nucleophilicity. Please explain your answer.
Rank the following set of compounds in order of increasing leaving group abililty in an addition and elimination mechanism (poorest leaving group at the left, best leaving group to the right). leaving group ability in an addition and Rank the following set of compounds in order of i elimination mechanism (poorest leaving group at the left, best leaving group to the right). NH2 OCH3 CI Best leaving group Poorest leaving group
5) Arrange the following ions in order of increasing nucleophilicity and leaving group ability. Please explain your answer by discussing the influence of the resonance and inductive effects
Rank the following alkyl bromides in order of decreasing reactivity to S2 substitution, by entering a ranking number (1-4) next to each structure (1=most reactive). Br-CHE Rank the following carbocations in order of decreasing stability, by entering a ranking number (1-3) in the space next to the structure (1-most stable). We were unable to transcribe this imageRank the following nucleophiles in decreasing order of nucleophilicity (most reactive first) in an aprotic solvent, by entering a ranking number (1-4) next to...
7.49 Rank the anions in order of increasing nucleophilicity in acetone: CH,S", CH NH", I, Br", and CH30 7.50 Classify each solvent as protic or aprotic. a. (CH CHOH C. CH CI2 @, NỊCH, b. CH.NO, d. NHA f. HCONH, than thoamide N atom in CH.CONHCH.CH.CH NHCH.?
show all work please thank you!!! 2. (4 pts total, 2 pts each) Rank the following compounds in order of increasing Brönsted acidity (1 = strongest acid, 3 = weakest acid and 2 = the one in the middle) a. CH3CO2H CH3CH2CHO CH3CH2OH b. CH3CH2NH2 CH3CH2OH CH3CH2SH
Rank the following molecules in order of basicity starting with the strongest base. [8 points] a) NH2 CH Br HN A B C D > > > strongest base weakest base
Rank the following group of alkanes in order of increasing boiling point.