updates now or try tonight? ACROSS DOWN 1 1) BH3 followed by 2) H202;NaOH are 2

Question

updates now or try tonight? ACROSS DOWN 1 1) BH3 followed by 2) H202;NaOH are 2 Most stable carbocation 5 This groups gets priority when naming the reagents used to give you a double or triple bonds. substituted alcohol 7 The pi bond in alkenes and alkynes act3 THis type of cation is when you have a as a positively charged carbon adjacent to a 9 Positively charged carbon double bond 10 When only one of two possible products 13 This catalyst is used to make cis alkenes 14 Rule that states the nucleophile goes to 15 (two words) This reagent is used to 17 KMnO4 in acid produces 18 Type of diene that contains alternating 4 The name of the ion intermediate when can be formed starting with an alkyne. the most substituted carbon extend the carbon chain on an alkyne containing compounds single and double bonds. Br2 reacts with an alkene 6 Enols are not stable and quickly form 8 KMnO4 in NaOH is used to make 10 The more of this you have the more stable the intermediate 11 This reagent removes terminal hydrogens on alkynes 12 Least stable carbocation. 16 An OH group attached to an alkene is called an

Explanation / Answer

Across

2. Tertiary ( tertiary carbocation is the most stable)

5. Alkyne ( triple bond gets the most priority)

7. Nucleophile

9. Carbocation

13. Lindlar's

18. Conjugated

Down

3. Allylic

4. Bromonium

6. Ketones

10. Resonance

12. Primary

16. Enol

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