Can someone please help me with this? Thank you! Chapter 4 McMurray ACROSS DOWN

Question

Can someone please help me with this? Thank you!

Chapter 4 McMurray 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 3 THis type of cation is when you have a 7 The pi bond in alkenes and alkynes act as a positively charged carbon adjacent to a 9 Positively charged carbon double bond 4 The name of the ion intermediate when 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 can be formed 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 starting with an alkyne the most substituted carbon extend the carbon chain on an alkyne containing compounds single and double bonds 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 carbocation

5. Double bond gets priority

7. Nucleophile

13. Lindlar's

9. Carbocation

14. Markovnikov's rule

15. Organometallic reagent

17.

18. Conjugated

Down:

1. Less substituted

3. anionic

4. Bromonium

12. Primary

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