Description : An electrophile acts as a __________ when it reacts with a nucleophile. (a) Bronsted-Lowry base (b) Arrhenius base (c) Lewis acid (d) Lewis base
Last Answer : Lewis acid
Description : Which is defined as a species that accepts a proton? (a) Lewis acid (b) Lewis base (c) Bronsted-Lowry acid (d) Bronsted-Lowry base
Last Answer : Bronsted-Lowry base
Description : A substance that accepts an electron pair is classified as a: w) bronsted-lowry acid x) bronsted-lowry base y) lewis acid z) lewis base
Last Answer : ANSWER: Y -- LEWIS ACID
Description : Any species that acts as an electron-pair acceptor a: w) Lewis base x) Bronsted base y) Lewis acid z) Bronsted acid
Description : In the reaction of propene with HCl, H+ ion acts as the : (a) electrophile (b) carbonium ion (c) nucleophile (d) carbanion
Last Answer : electrophile
Description : A compound which is an electron pair donor is generally classified as a: w) Lewis acid x) Bronsted base y) Bronsted acid z) Lewis base
Last Answer : ANSWER: Z -- LEWIS BASE
Description : Which of the following statements is incorrect? (a) Electrons move toward positively charged locations. (b) An electron-rich atom is called an electrophile. (c) An electrophile is electron loving. (d) A nucleophile has a a pair of electrons it can share
Last Answer : An electron-rich atom is called an electrophile.
Description : Which among the following compounds behave both as an electrophile as well a nucleophile? `{:(underset("(1)")(CH_(2)=CH_(2))" "underset("(2)")(CH_(2)=
Last Answer : Which among the following compounds behave both as an electrophile as well a nucleophile? `{:(underset("(1)")(CH_(2)= ... and (4) D. (2), (3) and (4)
Description : Which one of the following behaves both as a nucleophile and an electrophile ?
Last Answer : Which one of the following behaves both as a nucleophile and an electrophile ? A. `CH_(3)NH_(2)` B. `CH_(3)OH` C. `CH_(3)CN` D. `CH_(3)Cl`
Description : Identify a species which is not a Bronsted acid but a Lewis acid:
Last Answer : Identify a species which is not a Bronsted acid but a Lewis acid: A. HCl B. `NH_(3)` C. `BF_(3)` D. `H_(3)^(+)O`
Description : When semicarbazide reacts with a ketone (or aldehyde) to form semicarbazone. Only one nitrogen atom of semicarbazide acts as a nucleophile and attack
Last Answer : When semicarbazide reacts with a ketone (or aldehyde) to form semicarbazone. Only one ... atoms of semicarbazide are relatively non nucleophilic ?
Description : Which of the following statements correctly describes the general reactivity of alkynes? (a) An alkyne is an electron-rich molecule and therefore reacts as a nucleophile. (b) The σ bonds ... fail to undergo electrophilic addition reactions. (d) Alkynes are generally more reactive than alkenes.
Last Answer : Alkynes are generally more reactive than alkenes.
Description : How degree of ionization effects the strength of an acid or base according to Arrhenius concept?
Last Answer : Ans: An acid or base which will ionize completely, having high degree of ionization, will give more H+ or –OH ions. And will be a strong acid or base.
Description : Do you expect the carbon hydride of the type (CnH2n+2) to acts as Lewis acid or bases? Justify your answer
Last Answer : Ans: carbon hydride of the types(CnH2n+2)are electron-precise hydrides. In other words they have exact number of electron to form covalent bonds therefore they do not show any tendency to either gain or lose electron hence they are neither Lewis acid or Lewis bases.
Description : Which of the following is stronger Bronsted base?
Last Answer : Which of the following is stronger Bronsted base? A. B. C. D.
Description : Which of the following is the weakest Bronsted base?
Last Answer : Which of the following is the weakest Bronsted base? A. B. C. D.
Description : Which of the following is the strongest Bronsted base?
Last Answer : Which of the following is the strongest Bronsted base? A. B. C. D.
Description : Is h20 a bronsted base?
Last Answer : Feel Free to Answer
Description : What purpose does FeCl3 serve in the electrophilic aromatic substitution reaction between chlorine and benzene? (a) It serves as a radical initiator to produce the chlorine radical needed to propagate the ... by reacting with the Cl2 and thereby activates it toward attack by benzene's π electrons.
Last Answer : It serves as a Lewis acid catalyst by reacting with the Cl2 and thereby activates it toward attack by benzene’s π electrons.
Description : _______ Lewis Acid - Base Complexation Chemistry includes all the common mineral acids. (a) Type – 1 (b) Type – 2 (c) Type – 3 (d) Type – 4
Last Answer : (c) Type – 3
Description : Consider the coordination compound , `[Co(NH_(3))_(6)]Cl_(3)`. In the formation of the complex, the species which acts as the Lewis acid is :
Last Answer : Consider the coordination compound , `[Co(NH_(3))_(6)]Cl_(3)`. In the formation of the complex, the species which ... -)` C. `Co^(3+)` D. `NH_(3)`
Description : What characterize an Arrhenius base?
Last Answer : It Produces a hydroxide ion
Description : Which of the following is the stongest Bronsted acid?
Last Answer : Which of the following is the stongest Bronsted acid? A. B. C. D.
Description : An Arrhenius acid is a substance that: w) donates protons x) accepts protons y) donates hydrogen ions to water z) donates hydroxide ions to water
Last Answer : ANSWER: Y -- DONATES HYDROGEN IONS TO WATER
Description : "The rate at which a substance reacts is proportional to its active mass and the rate of a chemical reaction is proportional to the product of active masses of the reacting substances". This is the (A) Lewis- ... (B) Statement of Van't Hoff Equation (C) Le-Chatelier's principle (D) None of these
Last Answer : (D) None of these
Description : Ammonia can be considered a Lewis base because it can donate: w) electrons x) protons y) hydronium ions z) hydroxide ions
Last Answer : ANSWER: A -- ELECTRONS
Description : whats the climaxs in the book messenger by lois lowry
Last Answer : Need Answer
Description : How old is Lois Lowry is 2018?
Last Answer : What is the answer ?
Description : What are three adjectives that describe lois lowry' writing?
Last Answer : Pretentious and wordy.
Description : Electron-withdrawing groups are meta directors because : (a) the carbonium ion intermediate has a negative charge on the meta position. (b) the more stable resonance hybrid occurs with meta ... the electrophile. (d) the carbonium ion intermediate has a positive charge on the meta position
Last Answer : the more stable resonance hybrid occurs with meta attachment of the electrophile.
Description : Which of the following is not correct concerning substitution and elimination reactions of alkyl halides? (a) The electrophile replaces the leaving group. (b) Compounds containing electron-donating groups bonded to an ... replaced by another atom or group in substitution reactions. (d) (a) and (b)
Last Answer : (a) and (b)
Description : Which of the following is not an electrophile? (a) NH3 (b) Br+ (c) AlCl3 (d) NO2+
Last Answer : NH3
Description : Arrhenius equation represents graphically the variation between the __________ and temperature. (A) Rate of reaction (B) Frequency factor (C) Rate constant (D) Activation energy
Last Answer : (C) Rate constant
Description : Arrhenius equation shows the variation of __________ with temperature. (A) Reaction rate (B) Rate constant (C) Energy of activation (D) Frequency factor
Last Answer : (B) Rate constant
Description : Why cyanide ion act as ambident nucleophile ?
Last Answer : Ans.---- Cyanide ion can link through either carbon or nitrogen, therefore it is an ambident nuclophile.
Description : Which of the following is not a correct statement about the electrophilic substitution mechanism of benzene? (a) Benzene functions as a nucleophile. (b) Formation of a carbocation intermediate is the ... hybridized carbon in the ring. (d) The addition product is a frequently observed minor product.
Last Answer : The addition product is a frequently observed minor product.
Description : Why do aldehydes undergo nucleophilic addition reactions while esters undergo nucleophilic acyl substitution reactions? (a) The carbonyl carbon of an ester is more electrophilic than that of an aldehyde. (b) ... adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic
Last Answer : Once the nucleophile adds to an aldehyde, neither H− nor R− can be eliminated since they are strongly basic
Description : Which of the following factors has no effect on the rate of SN1 reactions? (a) the nature of the alkyl halide (b) the nature of the leaving group (c) the concentration of the alkyl halide (d) the concentration of the nucleophile
Last Answer : the concentration of the nucleophile
Description : Which of the following is the rate law for SN1 mechanisms? (a) Rate = k[Alkyl Halide] [Nucleophile] (b) Rate = k[Nucleophile] (c) Rate = k[Alkyl Halide] (d) Rate = k1[Alkyl Halide] + k2[Nucleophile]
Last Answer : Rate = k[Alkyl Halide]
Description : Which of the following is the best nucleophile in water? (a) I– (b) CH3SCH3 (c) CH3OCH3 (d) Cl–
Last Answer : I–
Description : Which of the following is the strongest nucleophile in an aqueous solution? (a) HO– (b) Cl– (c) Br– (d) I
Description : Which of the following statements concerning SN2 reactions of alkyl halides is not correct? (a) The rate of reaction depends on the concentration of the nucleophile. (b) The rate of reaction depends on the ... carbon of the C-Br bond. (d) All alkyl iodides react more rapidly than all alkyl chlorides
Last Answer : All alkyl iodides react more rapidly than all alkyl chlorides
Description : Which of the following factors influence whether a reaction will proceed by an SN1, SN2, E1, or E2 mechanism? (a) Structure of the alkyl halide (b) Solvent (c) Concentration of reagents (d) Nature of the nucleophile (e) All of these
Last Answer : All of these
Description : Which of the following is not a possible reaction of a carbocation? (a) addition of a nucleophile (b) rearrangement to a more stable carbocation (c) addition of a proton to form an alkane (d) loss of a β-hydrogen to form an alkene
Last Answer : addition of a proton to form an alkane
Description : Why does a H+ ion attacking a carbon-carbon double bond add to the carbon with the least number of substituents? (a) the reaction is resonance stabilized. (b) the hybrid geometry favors this ... tends to attack stable centers of negative charge. (d) a more stable carbonium ion is generated.
Last Answer : a more stable carbonium ion is generated.
Description : Which of the following is not a nucleophile? (a) FeBr3 (b) Br– (c) NH3 (d) CH3OCH3
Last Answer : CH3OCH3
Description : Which of the following is not normally considered to be a nucleophile? (a) NH3 (b) CH3NH2 (c) HC≡C:– (d) CH3CH2+
Last Answer : CH3CH2+
Description : Which of the following is not a nucleophile? (a) NH3 (b) HSO3– (c) AlCl3 (d) HO–
Last Answer : AlCl3
Description : Which of the following is a nucleophile? (a) AlCl3 (b) H3O+ (c) BF3 (d) CN–
Last Answer : CN–