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1) Drawa valid Lewis structure for each compound below. y CH CHy Cig Fe eet ae uw me Coa CaC-¢- Cu 3 % HHH H a Aw. as oo CFC. CHAN ge 5% ae) oh cms, t pee fr aed, W-c-e- 3F H-C-c-d-c-n Peart ba BE add HHH OH W-e—G W \ 4 33m cHon ar, Seahs NB wot ve 3 i Hoe 4 aa # 1 3 52 H—-P-p HC = eh a b 2) Draw a valid Lewis structure for each compound below. Assume the atoms are arranged as shown. HCO,C! re) HB 8: 3) For each compound shown below, determine the number of hydrogen present on each carbon g 8 ~*~ Her = ON Carbon Jokes tne place of one H 4) Determine the hybridization of each non-hydrogen atom in the compounds below. 1 H gevor + 5p? A), SAL ll esp =i AS 3 genet =5°* a ) nee % groves = SP ee eee p Single bend, dowble or endl, triple bonds 5 ne end low paitenh 4 ie, Cant as one sme © is rol a seve. Axa, all wag’ ald ras tat Se ae 3 oe 6 sp Sp I. Fs a Rpt See Bipiot teteahedeel sebehedrel Ee “NS Hc—=C=CH, Je, ; eteahedeal Aetrahedea | Kiagor as wo they He t oe b etahedial * ‘ f tctrahedhel > 7 Aregenal finecr — Hriseeal Plencr elmer 6) Classify each bond using 6 and n. List the number of each bond type (ie. 1 6 & 2 w bonds) § © ur || Page 2of$ 7) For each bond indicated in the structures below, determine the orbitals that make up that particular bond ake oor Reece 9 SP-Op ‘i Ae webs J Get Ope } é ea i eras ne" Pa Gel Ist Sp Cpt pH Spe 5p ? Gos = ce-ch x, wer po =< a t th t we Poe Osp*-Cops OSPF ~Cop® Cop -Csp= Gp Coss Cp-Cp = 8) Consider the molecule shown below: deanna Rank the indicated bonds inorder of increasing bond length byl acsesb

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