omplete the mechanism for the keto-enol tautomerization shown using bonds, charges, nonbonding electron pairs, and curved rows (forward reaction only). Do not remove any pre-drawn bonds or lone pairs. step 1: enol form. Add curved arrows. Select Draw Templates More 3 Ĉ Step 3: complete the structure, then add curved arrows. 020 Select Draw Templates More H: • 026 The tautomer that predominates in aqueous solution is the Oenol form. keto form. Step 2: complete the structure, then add curved arrows. Select Draw Templates More 4101 ! H Step 4: complete the keto form Select Draw Templates Mar Ć apa "I CM D: Qa

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Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.