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10£®Îª³ýÈ¥PbCrO4 ÖеÄSO42-ÔÓÖÊ£¬Ã¿´ÎÓÃ100mLÈ¥Àë×ÓˮϴµÓ£¬Ò»´ÎºÍÈý´ÎºóµÄËðʧ·Ö±ðÊÇ ( )

(A)£®1.7mg,5.1mg£» (B)£®0.017mg,0.051mg£» (C)£®0.17mg,3.4mg£» (D)£®0.17mg,5.1mg¡£ 11£®ÔÚŨ¶È¾ùΪ0.10 mol¡¤L-1µÄZn2+¡¢Cd2+¡¢Hg2+µÄ»ìºÏÈÜÒºÖУ¬[H+] = 2.0 mol¡¤L-1£¬ÏòÈÜÒºÖÐͨÈëH2SÖÁ±¥ºÍ£¬²»Éú³É³ÁµíµÄÀë×ÓÊÇ ( )

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12£®ÓûʹAg2CO3ת»¯ÎªAg2C2O4(Ksp= 5.3¡Á10-12)£¬±ØÐëʹ ( ) (A)£®[C2O42-] £¼ 0.63 [CO32-]£» (B)£®[C2O42-] £¾ 1.6[CO32-]£» (C)£®[C2O42-] £¼ 1.6 [CO32-]£» (D)£®[C2O42-] £¼ 0.63[CO32-]¡£

13£®In order to remove 90% of the Ag+ from a solution originally 0.10mol¡¤L-1 in Ag+,the [CrO42-] must be ( )

(A)£®1.12¡Á10-12; (B)£®1.12¡Á10-11; (C)£®1.12¡Á10-10; (D)£®1.12¡Á10-8. 14£®The addition of AgNO3 to a saturated solution of AgCl would ( ) (A)£®cause more AgCl to precipitate;

(B)£®.increase the solubility of AgCl due to the interionic attraction of NO3- and Ag+;

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(C)£®lower the value of Ksp for AgCl;

(D)£®.shift to the right the equilibrium AgCl(s) Ag+(aq) + Cl-(aq).

15£®To separate and identify the ions in a mixture that may contain Pb2+,Cu2+ and Mg2+, one might add the reagents H2S,HCl and NaOH, they should be added in the order. ( )

(A)£®HCl,H2S,NaOH; (B)£®H2S,HCl,NaOH; (C)£®HCl,NaOH,H2S; (D)£®NaOH,H2S,HCl.

16£®CrO42- is used as an indicator in the titration of Cl- with Ag+ because ( ) (A)£®it is yellow, whereas Cl- is colorless;

(B)£®Ag2CrO4, unlike AgCl is soluble in water; (C)£®Ag2CrO4 precipitates before AgCl;

(D)£®Ag2CrO4 precipitates only when virtually all the Cl- has reacted. ¢ç ¼ò´ðÌâ

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