Answer this simple Question The quantities provided were used for Step 1 in the synthesis of FeC₂O4 • 2 H₂O.(NH4)₂ [Fe(H₂O)6](SO4)2H₂C₂O4.2H₂O2.011.78Which reagent would be the limiting reagent?(NH4)₂[Fe(H₂O)](SO4)2H₂C₂O4.2H₂Otheoretical yield:Calculate the theoretical yield (in grams) of potassium trioxalatoferrate (III) trihydrate, K₂ [Fe(C₂O4)3].3 H₂O.6.0g What is added at the end of Step 2 to get the K3 [Fe(C₂O4)3] 3 H₂O to precipitate?O Hydrogen peroxideO Cold waterO Oxalic acid dehydrateEthanolOnce the crystals are on the filter paper in the Buchner funnel, why is the suction left on for a few minutes?To reduce the crystal sizeTo dry the filter paperO To 'seat' the filter paper in the funnelTo remove ethanol and dry the crystals

#Q.1: The balanced equation for thesynthesis of FeC2O4*2H2O is: (NH4)2[Fe(H2O)6](SO4)2(aq) +…

The quantities provided were used for Step 1 in the synthesis of FeC₂O4 • 2 H₂O. (NH₂)₂ [Fe(H₂O),](SO4)₂ H₂C₂04 2H₂O • Which reagent would be the limiting reagent? O H₂C₂O4 2H₂O 2.01 (NH4)₂[Fe(H₂O)6](SO4)₂ ● 1.78 theoretical yield: Calculate the theoretical yield (in grams) of potassium trioxalatoferrate (III) trihydrate, K₂ [Fe(C₂O)²]·3 H₂O. 9

The quantities provided were used for Step 1 in the synthesis of FeC₂O4 • 2 H₂O. (NH₂)₂ [Fe(H₂O),](SO4)₂ H₂C₂04 2H₂O • Which reagent would be the limiting reagent? O H₂C₂O4 2H₂O 2.01 (NH4)₂[Fe(H₂O)6](SO4)₂ ● 1.78 theoretical yield: Calculate the theoretical yield (in grams) of potassium trioxalatoferrate (III) trihydrate, K₂ [Fe(C₂O)²]·3 H₂O. 9

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Take a look at this molecule, and then answer the questions in the table below it. HOCH₂ HOCH₂ H H OH H H Explanation 0 O OH H OH H 0 H Is this a reducing sugar? OH Does this molecule contain a glycosidic bond? H If you said this molecule does contain a glycosidic bond, write the symbol describing it. If you said this molecule does contain a glycosidic bond, write the common names (including anomer and enantiomer labels) of the molecules that would be released if that bond were hydrolyzed. If there's more than one molecule, separate each name with a comma. Check Search A O yes Ono O yes O no 1 a X В W ローロ S © 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use Priv S
i need the answer quickly
condensed structural formula diagram for isopropylamine?
Decide whether the proposed Lewis structure below is reasonable. proposed Lewis structure Is this a reasonable structure? H H O Yes O No H H. H. H. H. O Yes T O)
See attached
Name the family to which each organic compound belongs. The first answer has been filled in for you. compound CH₂ || CH₂-C-0-C- CH₂ O || CH₂ || CH–C—NH, CH, OH I | CH₂-CH-C || || CH,—C–NH CH, X family ester 0
Draw the skeletal ("line") structure of N-methyl-3-hexanamine. Click and drag to start drawing a structure.
What is the name of this molecule?
Please answer the last 3 items only, 4-6.
Write the molecular formula for 1-butanol. Enter your answer in form of CxHyOz. Draw the structural formula for 1-butanol. C Draw Your Solution
CH3CO2(CH2)3CH3 = convert to complete structure
The prevalence of these organic substituents would indicate that a bio-molecule is a lipid? A) amide B) disulfide C) ester D) alcohol E) lots of hydrocarbons in rings or chains The prevalence of this organic functional group would indicate that a bio-molecule is a carbohydrate. A) amide B) disulfide C) ester D) alcohol E) lots of hydrocarbons in rings or chains